Product Details

SNP ID

rs201159012

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:74724716 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAAGTCCAAAGGTGGAATTTATC[A/C]TTTCAGGGGAATAGTCATTTCTTTT

Phenotype

MIM: 607009

Polymorphism

A/C, Transversion 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	5928	Missense Mutation	AGG,ATG	R1984M	NP_001170781.1
NM_001177311.1	5928	Missense Mutation	AGG,ATG	R1984M	NP_001170782.1
NM_017662.4	5928	Missense Mutation	AGG,ATG	R1989M	NP_060132.3
XM_011518244.1	5928	Missense Mutation	AGG,ATG	R1988M	XP_011516546.1
XM_011518245.1	5928	Missense Mutation	AGG,ATG	R1958M	XP_011516547.1
XM_011518246.1	5928	Missense Mutation	AGG,ATG	R1948M	XP_011516548.1
XM_011518247.1	5928	Missense Mutation	AGG,ATG	R1946M	XP_011516549.1
XM_011518248.1	5928	Missense Mutation	AGG,ATG	R1942M	XP_011516550.1
XM_011518249.1	5928	Missense Mutation	AGG,ATG	R1911M	XP_011516551.1
XM_011518250.1	5928	Missense Mutation	AGG,ATG	R1897M	XP_011516552.1
XM_011518251.2	5928	Missense Mutation	AGG,ATG	R1746M	XP_011516553.1
XM_011518252.2	5928	Intron			XP_011516554.1
XM_011518255.2	5928	Intron			XP_011516557.1
XM_017014287.1	5928	Missense Mutation	AGG,ATG	R1868M	XP_016869776.1
XM_017014288.1	5928	Missense Mutation	AGG,ATG	R1819M	XP_016869777.1
XM_017014289.1	5928	Intron			XP_016869778.1

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