Product Details

SNP ID

rs12989348

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:70150521 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGGAAGGATATCTGGGATCCACTC[A/G]ATGATGAAAGGTGTTGGCTCCTTTT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C2orf42 PubMed Links

Gene Details

Gene

C2orf42

Gene Name

chromosome 2 open reading frame 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017880.1	2081	Silent Mutation	ATC,ATT	I520I	NP_060350.1
XM_005264389.2	2081	Silent Mutation	ATC,ATT	I520I	XP_005264446.1
XM_005264390.2	2081	Silent Mutation	ATC,ATT	I520I	XP_005264447.1
XM_005264391.2	2081	Silent Mutation	ATC,ATT	I520I	XP_005264448.1
XM_011532937.2	2081	Silent Mutation	ATC,ATT	I520I	XP_011531239.1
XM_017004398.1	2081	Silent Mutation	ATC,ATT	I520I	XP_016859887.1
XM_017004399.1	2081	Silent Mutation	ATC,ATT	I520I	XP_016859888.1
XM_017004400.1	2081	Silent Mutation	ATC,ATT	I520I	XP_016859889.1

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