Product Details

SNP ID

rs61751870

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:127507078 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGGGGCCCCGTTGAGCAGGGGGC[C/T]GGCTGGTGGGGGGCTCTCAGGCCGC

Phenotype

MIM: 614045 MIM: 610933

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM129B PubMed Links

Gene Details

Gene

FAM129B

Gene Name

family with sequence similarity 129 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001035534.2	2039	Missense Mutation	AGC,GGC	S657G	NP_001030611.1
NM_022833.3	2039	Missense Mutation	AGC,GGC	S670G	NP_073744.2
XM_005252135.2	2039	Missense Mutation	AGC,GGC	S695G	XP_005252192.2
XM_011518925.1	2039	Missense Mutation	AGC,GGC	S700G	XP_011517227.1

Gene

LRSAM1

Gene Name

leucine rich repeat and sterile alpha motif containing 1

There are no transcripts associated with this gene.

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