Product Details

SNP ID: rs961362
Assay Type: Functionally tested
NCBI dbSNP Submissions: 29
Location: Chr.1:75800803 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GATACCTAAAGGTTTATGCCCAAGA[G/T]ATAGATATAGTGACCTGGAGCTACA
Phenotype: MIM: 602105 MIM: 179080
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: MSH4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002440.3		Intron			NP_002431.2

There are no transcripts associated with this gene.