Product Details

SNP ID

rs191262236

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:7766781 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCCAGGAAGTGAGGGCCCAGCTC[A/G]TCGTAATCAAAACTGCTGAGGAGCA

Phenotype

MIM: 605872

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLEC4M PubMed Links

Gene Details

Gene

CLEC4M

Gene Name

C-type lectin domain family 4 member M

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144904.1	959	Missense Mutation	ATC,GTC	I253V	NP_001138376.1
NM_001144905.1	959	Missense Mutation	ATC,GTC	I280V	NP_001138377.1
NM_001144906.1	959	Missense Mutation	ATC,GTC	I168V	NP_001138378.1
NM_001144907.1	959	Missense Mutation	ATC,GTC	I237V	NP_001138379.1
NM_001144908.1	959	Missense Mutation	ATC,GTC	I212V	NP_001138380.1
NM_001144909.1	959	Missense Mutation	ATC,GTC	I258V	NP_001138381.1
NM_001144910.1	959	Missense Mutation	ATC,GTC	I281V	NP_001138382.1
NM_001144911.1	959	Missense Mutation	ATC,GTC	I276V	NP_001138383.1
NM_014257.4	959	Missense Mutation	ATC,GTC	I304V	NP_055072.3
XM_006722611.2	959	Missense Mutation	ATC,GTC	I303V	XP_006722674.1
XM_006722612.3	959	Missense Mutation	ATC,GTC	I276V	XP_006722675.1
XM_006722613.3	959	Missense Mutation	ATC,GTC	I276V	XP_006722676.1
XM_006722614.3	959	Missense Mutation	ATC,GTC	I248V	XP_006722677.1
XM_006722615.2	959	Missense Mutation	ATC,GTC	I304V	XP_006722678.1

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