Product Details

SNP ID: rs148126792
Assay Type: Functionally tested
NCBI dbSNP Submissions: 3
Location: Chr.1:23362258 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AATTTTCTGGTGTGTGATGAGATGA[C/G]AGCTCCGGCTGAAGCTTTTCCCACA
Phenotype: MIM: 611703
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: ZNF436 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077195.1	1683	Missense Mutation	TCT,TGT	S375C	NP_001070663.1
NM_030634.2	1683	Missense Mutation	TCT,TGT	S375C	NP_085137.1
XM_011542201.1	1683	Missense Mutation	TCT,TGT	S357C	XP_011540503.1

There are no transcripts associated with this gene.