Product Details

SNP ID

rs143161006

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:74728322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATTGCATCTTCCCCCAAATTGGCC[A/G]GTCCAAACACCATTCCTCTTGATCT

Phenotype

MIM: 607009

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRPM6 PubMed Links

Gene Details

Gene

TRPM6

Gene Name

transient receptor potential cation channel subfamily M member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177310.1	5814	Missense Mutation	CCG,CTG	P1946L	NP_001170781.1
NM_001177311.1	5814	Missense Mutation	CCG,CTG	P1946L	NP_001170782.1
NM_017662.4	5814	Missense Mutation	CCG,CTG	P1951L	NP_060132.3
XM_011518244.1	5814	Missense Mutation	CCG,CTG	P1950L	XP_011516546.1
XM_011518245.1	5814	Missense Mutation	CCG,CTG	P1920L	XP_011516547.1
XM_011518246.1	5814	Missense Mutation	CCG,CTG	P1910L	XP_011516548.1
XM_011518247.1	5814	Missense Mutation	CCG,CTG	P1908L	XP_011516549.1
XM_011518248.1	5814	Missense Mutation	CCG,CTG	P1904L	XP_011516550.1
XM_011518249.1	5814	Missense Mutation	CCG,CTG	P1873L	XP_011516551.1
XM_011518250.1	5814	Missense Mutation	CCG,CTG	P1859L	XP_011516552.1
XM_011518251.2	5814	Missense Mutation	CCG,CTG	P1708L	XP_011516553.1
XM_011518252.2	5814	Intron			XP_011516554.1
XM_011518255.2	5814	Intron			XP_011516557.1
XM_017014287.1	5814	Missense Mutation	CCG,CTG	P1830L	XP_016869776.1
XM_017014288.1	5814	Missense Mutation	CCG,CTG	P1781L	XP_016869777.1
XM_017014289.1	5814	Intron			XP_016869778.1

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