Product Details

Primer Sequences

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Primer Chromosome Location

Chr.9: 74743938-74744199 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

TRPM6

Entrez Gene ID

140803

Gene Name

transient receptor potential cation channel subfamily M member 6

Gene Aliases

CHAK2, HMGX, HOMG, HOMG1, HSH

UniGene

Hs.272225

Gene Chromosome Location

Chr.9: 74722495-74888094 on Build GRCh38

Transcripts

NM_001177310.1 NM_001177311.1 NM_017662.4 XM_011518244.1 XM_011518245.1 XM_011518246.1 XM_011518247.1 XM_011518248.1 XM_011518249.1 XM_011518250.1 XM_011518251.2 XM_017014287.1 XM_017014288.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
5411253	c.5088C>T	p.I1696I	Chr.9: 74744141-74744141 on Build GRCh38
6809723	c.5116A>G	p.S1706G	Chr.9: 74744125-74744125 on Build GRCh38
6809594	c.5105G>T	p.S1702I	Chr.9: 74744124-74744124 on Build GRCh38
7149461	c.5095C>G	p.Q1699E	Chr.9: 74744119-74744119 on Build GRCh38
6809725	c.5116A>G	p.S1706G	Chr.9: 74744125-74744125 on Build GRCh38
6809595	c.5117G>T	p.S1706I	Chr.9: 74744124-74744124 on Build GRCh38
5411252	c.5100C>T	p.I1700I	Chr.9: 74744141-74744141 on Build GRCh38
4808764	c.5094A>T	p.S1698S	Chr.9: 74744147-74744147 on Build GRCh38
4736620	c.5097G>T	p.E1699D	Chr.9: 74744144-74744144 on Build GRCh38
6809592	c.5090G>T	p.S1697I	Chr.9: 74744124-74744124 on Build GRCh38
4736621	c.5085G>T	p.K1695N	Chr.9: 74744144-74744144 on Build GRCh38
5467744	c.5119+2T>C	p.?	Chr.9: 74744093-74744093 on Build GRCh38
7149460	c.5110C>G	p.Q1704E	Chr.9: 74744119-74744119 on Build GRCh38
7149464	c.5122C>G	p.Q1708E	Chr.9: 74744119-74744119 on Build GRCh38
3699817	c.5086A>C	p.K1696Q	Chr.9: 74744128-74744128 on Build GRCh38
4808763	c.5069-2A>T	p.?	Chr.9: 74744147-74744147 on Build GRCh38
6809620	c.5105C>T	p.A1702V	Chr.9: 74744136-74744136 on Build GRCh38
4736619	c.5070G>T	p.K1690N	Chr.9: 74744144-74744144 on Build GRCh38
6809724	c.5104A>G	p.S1702G	Chr.9: 74744125-74744125 on Build GRCh38
7149462	c.5095C>G	p.Q1699E	Chr.9: 74744119-74744119 on Build GRCh38
6809647	c.5070G>T	p.K1690N	Chr.9: 74744144-74744144 on Build GRCh38
6809722	c.5089A>G	p.S1697G	Chr.9: 74744125-74744125 on Build GRCh38
6809593	c.5117G>T	p.S1706I	Chr.9: 74744124-74744124 on Build GRCh38
4808765	c.5084-2A>T	p.?	Chr.9: 74744147-74744147 on Build GRCh38
6809618	c.5078C>T	p.A1693V	Chr.9: 74744136-74744136 on Build GRCh38
3699818	c.5113A>C	p.K1705Q	Chr.9: 74744128-74744128 on Build GRCh38
6809721	c.5089A>G	p.S1697G	Chr.9: 74744125-74744125 on Build GRCh38
6809648	c.5097G>T	p.E1699D	Chr.9: 74744144-74744144 on Build GRCh38
5411251	c.5073C>T	p.I1691I	Chr.9: 74744141-74744141 on Build GRCh38
5467746	c.5134+2T>C	p.?	Chr.9: 74744093-74744093 on Build GRCh38
1598488	c.5065A>C	p.I1689L	Chr.9: 74744176-74744176 on Build GRCh38
6809622	c.5105C>T	p.A1702V	Chr.9: 74744136-74744136 on Build GRCh38
5467745	c.5146+2T>C	p.?	Chr.9: 74744093-74744093 on Build GRCh38
5831122	c.5113A>C	p.K1705Q	Chr.9: 74744128-74744128 on Build GRCh38
6809621	c.5093C>T	p.A1698V	Chr.9: 74744136-74744136 on Build GRCh38
6809591	c.5090G>T	p.S1697I	Chr.9: 74744124-74744124 on Build GRCh38
1598487	c.5063T>C	p.V1688A	Chr.9: 74744178-74744178 on Build GRCh38
6809619	c.5078C>T	p.A1693V	Chr.9: 74744136-74744136 on Build GRCh38
7149463	c.5122C>G	p.Q1708E	Chr.9: 74744119-74744119 on Build GRCh38
3699819	c.5101A>C	p.K1701Q	Chr.9: 74744128-74744128 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs775951126	Chr.9: 74744056-74744056 on Build GRCh38
rs967851233	Chr.9: 74744025-74744025 on Build GRCh38
rs963952060	Chr.9: 74744087-74744087 on Build GRCh38
rs748124522	Chr.9: 74744072-74744072 on Build GRCh38
rs771038947	Chr.9: 74744163-74744163 on Build GRCh38
rs767669016	Chr.9: 74744124-74744124 on Build GRCh38
rs773201544	Chr.9: 74744077-74744077 on Build GRCh38
rs185242812	Chr.9: 74744074-74744074 on Build GRCh38
rs894606665	Chr.9: 74743991-74743991 on Build GRCh38
rs746540121	Chr.9: 74744051-74744051 on Build GRCh38
rs144525211	Chr.9: 74744053-74744053 on Build GRCh38
rs976983631	Chr.9: 74744117-74744117 on Build GRCh38
rs565181637	Chr.9: 74744007-74744007 on Build GRCh38
rs773933934	Chr.9: 74743990-74743990 on Build GRCh38
rs769785666	Chr.9: 74744076-74744076 on Build GRCh38
rs867161235	Chr.9: 74744104-74744104 on Build GRCh38
rs774611066	Chr.9: 74744085-74744085 on Build GRCh38
rs762840827	Chr.9: 74744082-74744082 on Build GRCh38
rs140493587	Chr.9: 74743993-74743993 on Build GRCh38
rs193058158	Chr.9: 74743992-74743992 on Build GRCh38
rs756625847	Chr.9: 74744164-74744164 on Build GRCh38
rs752709214	Chr.9: 74744136-74744136 on Build GRCh38
rs957955433	Chr.9: 74744058-74744058 on Build GRCh38
rs867452087	Chr.9: 74744122-74744122 on Build GRCh38
rs1055895466	Chr.9: 74743980-74743980 on Build GRCh38
rs761595871	Chr.9: 74744069-74744069 on Build GRCh38
rs575234607	Chr.9: 74744062-74744062 on Build GRCh38
rs766554589	Chr.9: 74744084-74744084 on Build GRCh38
rs759629217	Chr.9: 74744120-74744120 on Build GRCh38
rs557416219	Chr.9: 74743979-74743979 on Build GRCh38
rs764838440	Chr.9: 74744153-74744153 on Build GRCh38
rs989364206	Chr.9: 74744059-74744059 on Build GRCh38
rs998892907	Chr.9: 74744043-74744043 on Build GRCh38

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