Product Details

SNP ID

rs148732839

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:70809782 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGAATGGTGTCCCATCTGTCCAGC[A/G]CCAGGAGCCCTCTGTGCCCCTGTCA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLEC4F PubMed Links

Gene Details

Gene

CLEC4F

Gene Name

C-type lectin domain family 4 member F

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001258027.1	1692	Missense Mutation	CGC,TGC	R539C	NP_001244956.1
NM_001321308.1	1692	Missense Mutation	CGC,TGC	R539C	NP_001308237.1
NM_173535.2	1692	Missense Mutation	CGC,TGC	R539C	NP_775806.2
XM_011532635.2	1692	Missense Mutation	CGC,TGC	R649C	XP_011530937.1
XM_011532637.2	1692	Missense Mutation	CGC,TGC	R649C	XP_011530939.1
XM_011532638.2	1692	Missense Mutation	CGC,TGC	R649C	XP_011530940.1
XM_011532639.2	1692	Missense Mutation	CGC,TGC	R649C	XP_011530941.1
XM_011532640.2	1692	Missense Mutation	CGC,TGC	R649C	XP_011530942.1
XM_011532641.2	1692	UTR 3			XP_011530943.1
XM_011532642.2	1692	Missense Mutation	CGC,TGC	R509C	XP_011530944.1
XM_011532643.1	1692	Missense Mutation	CGC,TGC	R478C	XP_011530945.1
XM_017003519.1	1692	Missense Mutation	CGC,TGC	R649C	XP_016859008.1

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