Product Details

Primer Sequences

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Primer Chromosome Location

Chr.1: 111776060-111776313 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

KCND3

Entrez Gene ID

3752

Gene Name

potassium voltage-gated channel subfamily D member 3

Gene Aliases

BRGDA9, KCND3L, KCND3S, KSHIVB, KV4.3, SCA19, SCA22

UniGene

Hs.666367

Gene Chromosome Location

Chr.1: 111770662-111989577 on Build GRCh38

Transcripts

NM_004980.4 NM_172198.2 XM_005270851.4 XM_006710629.3 XM_006710630.3 XM_006710631.3 XM_017001244.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
3471289	c.1799G>A	p.G600E	Chr.1: 111776246-111776246 on Build GRCh38
4420108	c.1805G>C	p.R602T	Chr.1: 111776240-111776240 on Build GRCh38
1332732	c.1863G>A	p.T621T	Chr.1: 111776125-111776125 on Build GRCh38
7305336	c.1737C>T	p.D579D	Chr.1: 111776251-111776251 on Build GRCh38
4859616	c.1813T>A	p.C605S	Chr.1: 111776232-111776232 on Build GRCh38
4532380	c.1879G>A	p.G627R	Chr.1: 111776166-111776166 on Build GRCh38
893883	c.1758C>T	p.C586C	Chr.1: 111776230-111776230 on Build GRCh38
893882	c.1819G>A	p.E607K	Chr.1: 111776169-111776169 on Build GRCh38
6057529	c.1965G>T	p.L655F	Chr.1: 111776080-111776080 on Build GRCh38
4878958	c.1740C>T	p.D580D	Chr.1: 111776248-111776248 on Build GRCh38
4020656	c.1911C>T	p.G637G	Chr.1: 111776134-111776134 on Build GRCh38
893884	c.1745T>C	p.L582P	Chr.1: 111776243-111776243 on Build GRCh38
4876225	c.1958C>G	p.S653C	Chr.1: 111776087-111776087 on Build GRCh38
4020660	c.1798G>A	p.G600R	Chr.1: 111776247-111776247 on Build GRCh38
7305335	c.1794C>T	p.D598D	Chr.1: 111776251-111776251 on Build GRCh38
4020658	c.1807C>G	p.P603A	Chr.1: 111776238-111776238 on Build GRCh38
2119655	c.1960G>A	p.A654T	Chr.1: 111776085-111776085 on Build GRCh38
4878957	c.1797C>T	p.D599D	Chr.1: 111776248-111776248 on Build GRCh38
2119659	c.1887T>G	p.S629R	Chr.1: 111776158-111776158 on Build GRCh38
6835240	c.1841C>G	p.P614R	Chr.1: 111776147-111776147 on Build GRCh38
2119657	c.1889G>A	p.R630Q	Chr.1: 111776156-111776156 on Build GRCh38
674329	c.1756T>A	p.C586S	Chr.1: 111776232-111776232 on Build GRCh38
1127479	c.1901C>G	p.S634C	Chr.1: 111776087-111776087 on Build GRCh38
4420109	c.1748G>C	p.R583T	Chr.1: 111776240-111776240 on Build GRCh38
3471290	c.1742G>A	p.G581E	Chr.1: 111776246-111776246 on Build GRCh38
3471288	c.1781C>T	p.A594V	Chr.1: 111776207-111776207 on Build GRCh38
2119658	c.1832G>A	p.R611Q	Chr.1: 111776156-111776156 on Build GRCh38
4532381	c.1822G>A	p.G608R	Chr.1: 111776166-111776166 on Build GRCh38
2119656	c.1903G>A	p.A635T	Chr.1: 111776085-111776085 on Build GRCh38
7095127	c.1819G>C	p.E607Q	Chr.1: 111776169-111776169 on Build GRCh38
2119660	c.1830T>G	p.S610R	Chr.1: 111776158-111776158 on Build GRCh38
4020657	c.1854C>T	p.G618G	Chr.1: 111776134-111776134 on Build GRCh38
6835239	c.1898C>G	p.P633R	Chr.1: 111776147-111776147 on Build GRCh38
4020661	c.1741G>A	p.G581R	Chr.1: 111776247-111776247 on Build GRCh38
4020659	c.1750C>G	p.P584A	Chr.1: 111776238-111776238 on Build GRCh38
6057530	c.1908G>T	p.L636F	Chr.1: 111776080-111776080 on Build GRCh38
3471287	c.1838C>T	p.A613V	Chr.1: 111776207-111776207 on Build GRCh38
1583236	c.1876G>A	p.E626K	Chr.1: 111776169-111776169 on Build GRCh38
7095126	c.1876G>C	p.E626Q	Chr.1: 111776169-111776169 on Build GRCh38
1583235	c.1802T>C	p.L601P	Chr.1: 111776243-111776243 on Build GRCh38
3471286	c.1920G>A	p.T640T	Chr.1: 111776125-111776125 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs895254433	Chr.1: 111776189-111776189 on Build GRCh38
rs201275860	Chr.1: 111776204-111776204 on Build GRCh38
rs745523741	Chr.1: 111776248-111776248 on Build GRCh38
rs751182609	Chr.1: 111776203-111776203 on Build GRCh38
rs777172603	Chr.1: 111776128-111776128 on Build GRCh38
rs149344567	Chr.1: 111776247-111776247 on Build GRCh38
rs372362132	Chr.1: 111776166-111776166 on Build GRCh38
rs766650482	Chr.1: 111776179-111776179 on Build GRCh38
rs757457679	Chr.1: 111776084-111776085 on Build GRCh38
rs760710842	Chr.1: 111776169-111776169 on Build GRCh38
rs113196892	Chr.1: 111776249-111776249 on Build GRCh38
rs766562520	Chr.1: 111776102-111776102 on Build GRCh38
rs772579682	Chr.1: 111776163-111776163 on Build GRCh38
rs758286812	Chr.1: 111776127-111776127 on Build GRCh38
rs199663609	Chr.1: 111776180-111776180 on Build GRCh38
rs903701604	Chr.1: 111776273-111776273 on Build GRCh38
rs750478656	Chr.1: 111776098-111776098 on Build GRCh38
rs760907112	Chr.1: 111776099-111776099 on Build GRCh38
rs746497556	Chr.1: 111776132-111776132 on Build GRCh38
rs754759010	Chr.1: 111776121-111776121 on Build GRCh38
rs748519692	Chr.1: 111776277-111776277 on Build GRCh38
rs147087785	Chr.1: 111776086-111776086 on Build GRCh38
rs948125814	Chr.1: 111776196-111776196 on Build GRCh38
rs190953266	Chr.1: 111776109-111776109 on Build GRCh38
rs753669886	Chr.1: 111776103-111776103 on Build GRCh38
rs774711788	Chr.1: 111776085-111776085 on Build GRCh38
rs752589615	Chr.1: 111776126-111776126 on Build GRCh38
rs772493153	Chr.1: 111776280-111776280 on Build GRCh38
rs910058506	Chr.1: 111776108-111776108 on Build GRCh38
rs147262533	Chr.1: 111776155-111776155 on Build GRCh38
rs939370048	Chr.1: 111776162-111776162 on Build GRCh38
rs779007324	Chr.1: 111776212-111776212 on Build GRCh38
rs758318696	Chr.1: 111776186-111776186 on Build GRCh38
rs375391961	Chr.1: 111776243-111776243 on Build GRCh38
rs777736918	Chr.1: 111776200-111776200 on Build GRCh38
rs762261334	Chr.1: 111776158-111776158 on Build GRCh38
rs752495973	Chr.1: 111776184-111776184 on Build GRCh38
rs774713377	Chr.1: 111776156-111776156 on Build GRCh38
rs181971539	Chr.1: 111776251-111776251 on Build GRCh38
rs780988439	Chr.1: 111776148-111776148 on Build GRCh38
rs770747636	Chr.1: 111776140-111776140 on Build GRCh38
rs767502190	Chr.1: 111776097-111776097 on Build GRCh38
rs773760801	Chr.1: 111776284-111776284 on Build GRCh38
rs756814713	Chr.1: 111776223-111776223 on Build GRCh38
rs944024237	Chr.1: 111776167-111776167 on Build GRCh38
rs186194682	Chr.1: 111776276-111776276 on Build GRCh38

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