Product Details

SNP ID

rs61734441

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:6501817 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCAAACTTGTCCTCGCTAGAGGG[A/G]GAAATGCTCTGGCAGGCATCCTGTA

Phenotype

MIM: 610639

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GRID2IP PubMed Links

Gene Details

Gene

GRID2IP

Gene Name

Grid2 interacting protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145118.1	3363	Silent Mutation	TCC,TCT	S1121S	NP_001138590.1
XM_011515404.2	3363	Silent Mutation	TCC,TCT	S937S	XP_011513706.1

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