Product Details

Primer Sequences

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Primer Chromosome Location

Chr.10: 59264032-59264287 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

FAM13C

Entrez Gene ID

220965

Gene Name

family with sequence similarity 13 member C

Gene Aliases

FAM13C1

UniGene

Hs.607594

Gene Chromosome Location

Chr.10: 59245933-59363186 on Build GRCh38

Transcripts

NM_001001971.2 NM_001143773.1 NM_001166698.1 NM_198215.3 XM_005269618.4 XM_005269619.4 XM_006717702.3 XM_006717703.3 XM_011539490.2 XM_011539491.2 XM_017015885.1 XM_017015886.1 XM_017015887.1 XM_017015888.1 XM_017015889.1 XM_017015890.1 XM_017015891.1 XM_017015892.1 XM_017015893.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
4814927	c.1010G>C	p.R337P	Chr.10: 59264099-59264099 on Build GRCh38
1474680	c.1010G>C	p.R337P	Chr.10: 59264099-59264099 on Build GRCh38
1702476	c.944C>T	p.P315L	Chr.10: 59264165-59264165 on Build GRCh38
3439135	c.987G>A	p.W329*	Chr.10: 59264122-59264122 on Build GRCh38
3807398	c.967A>C	p.N323H	Chr.10: 59264142-59264142 on Build GRCh38
3439137	c.981G>A	p.L327L	Chr.10: 59264128-59264128 on Build GRCh38
1702477	c.944C>T	p.P315L	Chr.10: 59264165-59264165 on Build GRCh38
5896062	c.994G>A	p.D332N	Chr.10: 59264115-59264115 on Build GRCh38
3439136	c.987G>A	p.W329*	Chr.10: 59264122-59264122 on Build GRCh38
3397190	c.980T>C	p.L327P	Chr.10: 59264129-59264129 on Build GRCh38
3439138	c.981G>A	p.L327L	Chr.10: 59264128-59264128 on Build GRCh38
6461235	c.963T>G	p.T321T	Chr.10: 59264146-59264146 on Build GRCh38
3807397	c.967A>C	p.N323H	Chr.10: 59264142-59264142 on Build GRCh38
3415134	c.1009C>T	p.R337C	Chr.10: 59264100-59264100 on Build GRCh38
1675260	c.994G>T	p.D332Y	Chr.10: 59264115-59264115 on Build GRCh38
3415135	c.1009C>T	p.R337C	Chr.10: 59264100-59264100 on Build GRCh38
5896061	c.994G>A	p.D332N	Chr.10: 59264115-59264115 on Build GRCh38
3397191	c.980T>C	p.L327P	Chr.10: 59264129-59264129 on Build GRCh38
1675259	c.994G>T	p.D332Y	Chr.10: 59264115-59264115 on Build GRCh38
6461236	c.963T>G	p.T321T	Chr.10: 59264146-59264146 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs753235458	Chr.10: 59264180-59264181 on Build GRCh38
rs371436185	Chr.10: 59264224-59264224 on Build GRCh38
rs772920908	Chr.10: 59264137-59264137 on Build GRCh38
rs990216153	Chr.10: 59264128-59264128 on Build GRCh38
rs137976326	Chr.10: 59264100-59264100 on Build GRCh38
rs544577803	Chr.10: 59264251-59264251 on Build GRCh38
rs71467058	Chr.10: 59264224-59264225 on Build GRCh38
rs538115420	Chr.10: 59264068-59264068 on Build GRCh38
rs748499961	Chr.10: 59264064-59264064 on Build GRCh38
rs375175726	Chr.10: 59264147-59264147 on Build GRCh38
rs780891400	Chr.10: 59264060-59264060 on Build GRCh38
rs766288018	Chr.10: 59264176-59264176 on Build GRCh38
rs771497792	Chr.10: 59264078-59264078 on Build GRCh38
rs778874102	Chr.10: 59264099-59264099 on Build GRCh38
rs755787039	Chr.10: 59264204-59264204 on Build GRCh38
rs376187928	Chr.10: 59264190-59264190 on Build GRCh38
rs762887683	Chr.10: 59264156-59264156 on Build GRCh38
rs538838463	Chr.10: 59264223-59264223 on Build GRCh38
rs752416394	Chr.10: 59264201-59264201 on Build GRCh38
rs368817959	Chr.10: 59264067-59264067 on Build GRCh38
rs556346617	Chr.10: 59264076-59264076 on Build GRCh38
rs71467059	Chr.10: 59264231-59264232 on Build GRCh38
rs372071096	Chr.10: 59264120-59264120 on Build GRCh38
rs749845319	Chr.10: 59264077-59264077 on Build GRCh38
rs759053855	Chr.10: 59264192-59264192 on Build GRCh38
rs767122140	Chr.10: 59264193-59264193 on Build GRCh38
rs35958081	Chr.10: 59264226-59264227 on Build GRCh38
rs769603713	Chr.10: 59264131-59264131 on Build GRCh38
rs751094395	Chr.10: 59264188-59264188 on Build GRCh38
rs766314585	Chr.10: 59264058-59264059 on Build GRCh38

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