Product Details

SNP ID

rs1192794

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:101281760 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTACTCTTCGATAGCTCAAACTCGA[A/G]CAATCCTCCCACCTTAAACTCCCAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF149 PubMed Links

Gene Details

Gene

RNF149

Gene Name

ring finger protein 149

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173647.3	1057	Intron			NP_775918.2
XM_005263920.2	1057	Missense Mutation	CTC,TTC	L420F	XP_005263977.1
XM_005263921.3	1057	Intron			XP_005263978.1
XM_011510990.2	1057	Missense Mutation	CTC,TTC	L259F	XP_011509292.1

Gene

SNORD89

Gene Name

small nucleolar RNA, C/D box 89

There are no transcripts associated with this gene.

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