Product Details

SNP ID

rs36117362

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:93726401 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTATCATTACAATAGGTTTTCC[A/G]AAATTCTCTGTATGCACCAGATTAT

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	10929	Intron			NP_001269963.1
NM_145269.4	10929	Intron			NP_660312.2
XM_005250787.2	10929	Missense Mutation	CAA,CGA	Q152R	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	10929	Intron			NP_976324.2
XM_005250915.4	10929	Intron			XP_005250972.1
XM_011517027.2	10929	UTR 3			XP_011515329.1
XM_011517028.2	10929	Intron			XP_011515330.1
XM_011517029.2	10929	Intron			XP_011515331.1
XM_017013406.1	10929	Intron			XP_016868895.1
XM_017013407.1	10929	Intron			XP_016868896.1
XM_017013408.1	10929	Intron			XP_016868897.1

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