Product Details

SNP ID

rs2919347

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:65047546 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTGTGTTTGGTTTCTCAACTTCAA[C/T]ACTTTTCTTTGTGAGTTCAGGGGTT

Phenotype

MIM: 612085

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RASL12 PubMed Links

Gene Details

Gene

RASL12

Gene Name

RAS like family 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001307930.1		Intron			NP_001294859.1
NM_016563.3		Intron			NP_057647.1
XM_005254434.4		Intron			XP_005254491.1
XM_011521660.2		Intron			XP_011519962.1
XM_017022296.1		Intron			XP_016877785.1

Gene

SLC51B

Gene Name

solute carrier family 51 beta subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178859.3		Intron			NP_849190.2
XM_005254159.4		Intron			XP_005254216.1

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