Product Details

Primer Sequences

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Primer Chromosome Location

Chr.4: 54695642-54695805 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

KIT

Entrez Gene ID

3815

Gene Name

KIT proto-oncogene receptor tyrosine kinase

Gene Aliases

C-Kit, CD117, PBT, SCFR

UniGene

Hs.479754

Gene Chromosome Location

Chr.4: 54657928-54740715 on Build GRCh38

Transcripts

NM_000222.2 NM_001093772.1 XM_005265740.1 XM_005265741.1 XM_005265742.2 XM_017008178.1 XM_017008179.1 XM_017008180.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6494994	c.252G>T	p.T84T	Chr.4: 54695696-54695696 on Build GRCh38
1430109	c.288G>A	p.T96T	Chr.4: 54695732-54695732 on Build GRCh38
6983718	c.291delC	p.C97fs*1	Chr.4: 54695735-54695735 on Build GRCh38
1430110	c.303C>T	p.H101H	Chr.4: 54695747-54695747 on Build GRCh38
6437972	c.265G>A	p.A89T	Chr.4: 54695709-54695709 on Build GRCh38
3301421	c.200C>G	p.T67S	Chr.4: 54695644-54695644 on Build GRCh38
7345631	c.329_331delTTG	p.V111delV	Chr.4: 54695773-54695775 on Build GRCh38
6919223	c.217G>T	p.E73*	Chr.4: 54695661-54695661 on Build GRCh38
3661124	c.273C>A	p.N91K	Chr.4: 54695717-54695717 on Build GRCh38
3301422	c.252G>A	p.T84T	Chr.4: 54695696-54695696 on Build GRCh38
7306850	c.277G>A	p.G93S	Chr.4: 54695721-54695721 on Build GRCh38
6916741	c.208A>T	p.I70F	Chr.4: 54695652-54695652 on Build GRCh38
6934652	c.301C>A	p.H101N	Chr.4: 54695745-54695745 on Build GRCh38
1056093	c.304G>A	p.G102S	Chr.4: 54695748-54695748 on Build GRCh38
139519	c.304G>T	p.G102C	Chr.4: 54695748-54695748 on Build GRCh38
5636600	c.269C>G	p.T90S	Chr.4: 54695713-54695713 on Build GRCh38
6167412	c.270C>T	p.T90T	Chr.4: 54695714-54695714 on Build GRCh38
295951	c.276C>T	p.T92T	Chr.4: 54695720-54695720 on Build GRCh38
3301423	c.335G>T	p.R112I	Chr.4: 54695779-54695779 on Build GRCh38
6437987	c.221C>T	p.T74M	Chr.4: 54695665-54695665 on Build GRCh38
6924758	c.262G>A	p.E88K	Chr.4: 54695706-54695706 on Build GRCh38
4969012	c.286A>C	p.T96P	Chr.4: 54695730-54695730 on Build GRCh38
167171	c.222G>A	p.T74T	Chr.4: 54695666-54695666 on Build GRCh38
6437982	c.253G>T	p.E85*	Chr.4: 54695697-54695697 on Build GRCh38
3409366	c.216T>A	p.D72E	Chr.4: 54695660-54695660 on Build GRCh38
6529236	c.214G>C	p.D72H	Chr.4: 54695658-54695658 on Build GRCh38
3380948	c.251C>T	p.T84M	Chr.4: 54695695-54695695 on Build GRCh38
22225	c.217G>A	p.E73K	Chr.4: 54695661-54695661 on Build GRCh38
5546396	c.253G>A	p.E85K	Chr.4: 54695697-54695697 on Build GRCh38
22226	c.287C>T	p.T96M	Chr.4: 54695731-54695731 on Build GRCh38
6930003	c.198G>A	p.W66*	Chr.4: 54695642-54695642 on Build GRCh38
3849654	c.235C>A	p.Q79K	Chr.4: 54695679-54695679 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs150026676	Chr.4: 54695732-54695732 on Build GRCh38
rs146081659	Chr.4: 54695724-54695724 on Build GRCh38
rs781130745	Chr.4: 54695745-54695745 on Build GRCh38
rs750916458	Chr.4: 54695687-54695687 on Build GRCh38
rs867439564	Chr.4: 54695730-54695730 on Build GRCh38
rs780922356	Chr.4: 54695764-54695764 on Build GRCh38
rs779113666	Chr.4: 54695729-54695729 on Build GRCh38
rs145333060	Chr.4: 54695747-54695747 on Build GRCh38
rs56411694	Chr.4: 54695696-54695696 on Build GRCh38
rs769632130	Chr.4: 54695748-54695748 on Build GRCh38
rs904550523	Chr.4: 54695725-54695725 on Build GRCh38
rs959320112	Chr.4: 54695738-54695738 on Build GRCh38
rs1020222899	Chr.4: 54695705-54695705 on Build GRCh38
rs371353189	Chr.4: 54695674-54695674 on Build GRCh38
rs768599276	Chr.4: 54695741-54695741 on Build GRCh38
rs373066995	Chr.4: 54695720-54695720 on Build GRCh38
rs779652404	Chr.4: 54695761-54695761 on Build GRCh38
rs749024557	Chr.4: 54695763-54695763 on Build GRCh38
rs794726674	Chr.4: 54695697-54695697 on Build GRCh38
rs201872586	Chr.4: 54695695-54695695 on Build GRCh38

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