Product Details

SNP ID

rs201660346

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:93726505 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTGTCAGCTAAGTGTGTATCTGGA[A/G]CAGGACAGGTGAGCAAGAAACCGTA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM92A1 PubMed Links

Gene Details

Gene

FAM92A1

Gene Name

family with sequence similarity 92 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283034.1	10825	Intron			NP_001269963.1
NM_145269.4	10825	Intron			NP_660312.2
XM_005250787.2	10825	Missense Mutation	ACA,GCA	T187A	XP_005250844.1

Gene

RBM12B

Gene Name

RNA binding motif protein 12B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203390.2	10825	Intron			NP_976324.2
XM_005250915.4	10825	Intron			XP_005250972.1
XM_011517027.2	10825	UTR 3			XP_011515329.1
XM_011517028.2	10825	Intron			XP_011515330.1
XM_011517029.2	10825	Intron			XP_011515331.1
XM_017013406.1	10825	Intron			XP_016868895.1
XM_017013407.1	10825	Intron			XP_016868896.1
XM_017013408.1	10825	Intron			XP_016868897.1

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