Product Details

Primer Sequences

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Primer Chromosome Location

Chr.5: 157492892-157493157 on Build GRCh38 View in UCSC browser

Format

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer^™ Tool Quick Reference

Ampliseq ID's

Gene Details

Gene Symbol

ADAM19

Entrez Gene ID

8728

Gene Name

ADAM metallopeptidase domain 19

Gene Aliases

FKSG34, MADDAM, MLTNB

UniGene

Hs.483944

Gene Chromosome Location

Chr.5: 157477304-157575823 on Build GRCh38

Transcripts

NM_033274.4 XM_005266003.2 XM_011534682.2 XM_017010009.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6593473	c.1748G>A	p.R583Q	Chr.5: 157493133-157493133 on Build GRCh38
6593548	c.1840C>T	p.R614*	Chr.5: 157493047-157493047 on Build GRCh38
1150012	c.1755G>T	p.L585L	Chr.5: 157493126-157493126 on Build GRCh38
7102744	c.1764C>T	p.N588N	Chr.5: 157493117-157493117 on Build GRCh38
7305398	c.1835T>G	p.V612G	Chr.5: 157493052-157493052 on Build GRCh38
5720489	c.1774G>A	p.V592M	Chr.5: 157493113-157493113 on Build GRCh38
5798671	c.1766C>T	p.A589V	Chr.5: 157493115-157493115 on Build GRCh38
5094866	c.1771G>T	p.A591S	Chr.5: 157493116-157493116 on Build GRCh38
6170440	c.951C>G	p.P317P	Chr.5: 157493129-157493129 on Build GRCh38
4859396	c.955G>T	p.E319*	Chr.5: 157493125-157493125 on Build GRCh38
6593504	c.1015C>T	p.R339W	Chr.5: 157493065-157493065 on Build GRCh38
6103202	c.1858G>T	p.G620C	Chr.5: 157493029-157493029 on Build GRCh38
3947197	c.1767G>C	p.A589A	Chr.5: 157493114-157493114 on Build GRCh38
4859386	c.1761G>T	p.L587L	Chr.5: 157493126-157493126 on Build GRCh38
3246760	c.1772C>A	p.P591H	Chr.5: 157493109-157493109 on Build GRCh38
4346131	c.971C>A	p.P324H	Chr.5: 157493109-157493109 on Build GRCh38
5731209	c.1886G>A	p.G629E	Chr.5: 157492995-157492995 on Build GRCh38
3947199	c.966G>C	p.A322A	Chr.5: 157493114-157493114 on Build GRCh38
3853218	c.1770G>A	p.V590V	Chr.5: 157493111-157493111 on Build GRCh38
5662283	c.1840C>A	p.R614R	Chr.5: 157493047-157493047 on Build GRCh38
1319230	c.1791C>A	p.I597I	Chr.5: 157493090-157493090 on Build GRCh38
4516302	c.1773_1774GG>AA	p.V592M	Chr.5: 157493113-157493114 on Build GRCh38
6593547	c.1834C>T	p.R612*	Chr.5: 157493047-157493047 on Build GRCh38
3853219	c.1776G>A	p.V592V	Chr.5: 157493111-157493111 on Build GRCh38
7102746	c.1770C>T	p.N590N	Chr.5: 157493117-157493117 on Build GRCh38
1283252	c.1890C>A	p.T630T	Chr.5: 157492991-157492991 on Build GRCh38
6103203	c.1051G>T	p.G351C	Chr.5: 157493029-157493029 on Build GRCh38
4516301	c.1767_1768GG>AA	p.V590M	Chr.5: 157493113-157493114 on Build GRCh38
3853220	c.969G>A	p.V323V	Chr.5: 157493111-157493111 on Build GRCh38
7102747	c.963C>T	p.N321N	Chr.5: 157493117-157493117 on Build GRCh38
6885001	c.1882G>A	p.V628M	Chr.5: 157493005-157493005 on Build GRCh38
6885002	c.1075G>A	p.V359M	Chr.5: 157493005-157493005 on Build GRCh38
6593549	c.1033C>T	p.R345*	Chr.5: 157493047-157493047 on Build GRCh38
4346130	c.1778C>A	p.P593H	Chr.5: 157493109-157493109 on Build GRCh38
5798672	c.1772C>T	p.A591V	Chr.5: 157493115-157493115 on Build GRCh38
5731211	c.1085G>A	p.G362E	Chr.5: 157492995-157492995 on Build GRCh38
1150010	c.1756G>T	p.E586*	Chr.5: 157493125-157493125 on Build GRCh38
6170438	c.1752C>G	p.P584P	Chr.5: 157493129-157493129 on Build GRCh38
4859387	c.954G>T	p.L318L	Chr.5: 157493126-157493126 on Build GRCh38
5720490	c.967G>A	p.V323M	Chr.5: 157493113-157493113 on Build GRCh38
5731210	c.1892G>A	p.G631E	Chr.5: 157492995-157492995 on Build GRCh38
7305399	c.1028T>G	p.V343G	Chr.5: 157493052-157493052 on Build GRCh38
4859395	c.1762G>T	p.E588*	Chr.5: 157493125-157493125 on Build GRCh38
6593475	c.947G>A	p.R316Q	Chr.5: 157493133-157493133 on Build GRCh38
5662284	c.1033C>A	p.R345R	Chr.5: 157493047-157493047 on Build GRCh38
4531517	c.1804G>A	p.G602R	Chr.5: 157493083-157493083 on Build GRCh38
3947198	c.1773G>C	p.A591A	Chr.5: 157493114-157493114 on Build GRCh38
1672084	c.1876G>A	p.V626M	Chr.5: 157493005-157493005 on Build GRCh38
3853214	c.1835G>A	p.R612Q	Chr.5: 157493046-157493046 on Build GRCh38
6103201	c.1852G>T	p.G618C	Chr.5: 157493029-157493029 on Build GRCh38
6593503	c.1822C>T	p.R608W	Chr.5: 157493065-157493065 on Build GRCh38
5720488	c.1768G>A	p.V590M	Chr.5: 157493113-157493113 on Build GRCh38
5094865	c.1765G>T	p.A589S	Chr.5: 157493116-157493116 on Build GRCh38
3853216	c.1034G>A	p.R345Q	Chr.5: 157493046-157493046 on Build GRCh38
1186890	c.1817G>T	p.R606L	Chr.5: 157493064-157493064 on Build GRCh38
6170439	c.1758C>G	p.P586P	Chr.5: 157493129-157493129 on Build GRCh38
6593474	c.1754G>A	p.R585Q	Chr.5: 157493133-157493133 on Build GRCh38
3853215	c.1841G>A	p.R614Q	Chr.5: 157493046-157493046 on Build GRCh38
4531516	c.1798G>A	p.G600R	Chr.5: 157493083-157493083 on Build GRCh38
7305396	c.1829T>G	p.V610G	Chr.5: 157493052-157493052 on Build GRCh38
6593502	c.1816C>T	p.R606W	Chr.5: 157493065-157493065 on Build GRCh38
5662282	c.1834C>A	p.R612R	Chr.5: 157493047-157493047 on Build GRCh38
5798673	c.965C>T	p.A322V	Chr.5: 157493115-157493115 on Build GRCh38
4516303	c.966_967GG>AA	p.V323M	Chr.5: 157493113-157493114 on Build GRCh38
4531518	c.997G>A	p.G333R	Chr.5: 157493083-157493083 on Build GRCh38
5094867	c.964G>T	p.A322S	Chr.5: 157493116-157493116 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs776784665	Chr.5: 157493134-157493134 on Build GRCh38
rs199813857	Chr.5: 157492991-157492991 on Build GRCh38
rs752071144	Chr.5: 157493113-157493113 on Build GRCh38
rs749000395	Chr.5: 157493121-157493121 on Build GRCh38
rs779398349	Chr.5: 157492932-157492932 on Build GRCh38
rs745796954	Chr.5: 157493132-157493132 on Build GRCh38
rs762086190	Chr.5: 157493089-157493089 on Build GRCh38
rs774054863	Chr.5: 157493131-157493131 on Build GRCh38
rs1038412130	Chr.5: 157493000-157493000 on Build GRCh38
rs536691661	Chr.5: 157493030-157493030 on Build GRCh38
rs754020073	Chr.5: 157493074-157493074 on Build GRCh38
rs529559129	Chr.5: 157493133-157493133 on Build GRCh38
rs370590283	Chr.5: 157493117-157493117 on Build GRCh38
rs762744387	Chr.5: 157493039-157493039 on Build GRCh38
rs929872438	Chr.5: 157493054-157493054 on Build GRCh38
rs765560665	Chr.5: 157493095-157493095 on Build GRCh38
rs764108529	Chr.5: 157492963-157492963 on Build GRCh38
rs780604591	Chr.5: 157492992-157492992 on Build GRCh38
rs757594695	Chr.5: 157492929-157492929 on Build GRCh38
rs79025446	Chr.5: 157493114-157493114 on Build GRCh38
rs764203673	Chr.5: 157493065-157493065 on Build GRCh38
rs1046979607	Chr.5: 157493069-157493069 on Build GRCh38
rs769455423	Chr.5: 157493022-157493022 on Build GRCh38
rs561919833	Chr.5: 157493084-157493084 on Build GRCh38
rs747691760	Chr.5: 157493116-157493116 on Build GRCh38
rs11466785	Chr.5: 157492926-157492926 on Build GRCh38
rs770757234	Chr.5: 157493128-157493128 on Build GRCh38
rs770719684	Chr.5: 157493047-157493047 on Build GRCh38
rs747773326	Chr.5: 157493011-157493011 on Build GRCh38
rs780347101	Chr.5: 157493111-157493111 on Build GRCh38
rs750757281	Chr.5: 157493100-157493100 on Build GRCh38
rs780623373	Chr.5: 157492965-157492965 on Build GRCh38
rs758774350	Chr.5: 157493103-157493103 on Build GRCh38
rs759459737	Chr.5: 157493053-157493053 on Build GRCh38
rs751388553	Chr.5: 157493081-157493081 on Build GRCh38
rs758907205	Chr.5: 157492948-157492948 on Build GRCh38
rs777419913	Chr.5: 157493118-157493118 on Build GRCh38
rs909937897	Chr.5: 157493110-157493110 on Build GRCh38
rs761997923	Chr.5: 157493137-157493137 on Build GRCh38
rs373319182	Chr.5: 157492979-157492979 on Build GRCh38
rs1037019010	Chr.5: 157493122-157493122 on Build GRCh38
rs780699401	Chr.5: 157493115-157493115 on Build GRCh38
rs1049055617	Chr.5: 157493063-157493063 on Build GRCh38
rs750849006	Chr.5: 157492944-157492944 on Build GRCh38
rs768205295	Chr.5: 157492982-157492982 on Build GRCh38

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