Product Details

SNP ID
rs75505282
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:34493579 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCCTGGACGGGGTTCCCTTCACC[A/G]TGGACGTGGAGAACAACATCTACTG
Phenotype
MIM: 614790
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
WTIP PubMed Links

Gene Details

Gene
WTIP
Gene Name
Wilms tumor 1 interacting protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080436.1 422 Missense Mutation ATG,GTG M330V NP_001073905.1
XM_006723014.3 422 Missense Mutation ATG,GTG M330V XP_006723077.1
XM_011526452.2 422 Missense Mutation ATG,GTG M330V XP_011524754.1
XM_011526453.2 422 Missense Mutation ATG,GTG M89V XP_011524755.1

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