Product Details

SNP ID: rs7527057
Assay Type: Functionally tested
NCBI dbSNP Submissions: 42
Location: Chr.1:74706317 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATCATCATAAGAGAAGAATCATTTT[A/T]CCAGTAGCCCCACTACCATGAATGA
Phenotype: MIM: 123691
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: CRYZ PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130042.1	958	Silent Mutation	GGA,GGT	G323G	NP_001123514.1
NM_001130043.1	958	Silent Mutation	GGA,GGT	G289G	NP_001123515.1
NM_001134759.1	958	Silent Mutation	GGA,GGT	G186G	NP_001128231.1
NM_001889.3	958	Silent Mutation	GGA,GGT	G323G	NP_001880.2
XM_005270491.4	958	Silent Mutation	GGA,GGT	G186G	XP_005270548.1
XM_011540747.1	958	Silent Mutation	GGA,GGT	G323G	XP_011539049.1
XM_017000367.1	958	Silent Mutation	GGA,GGT	G289G	XP_016855856.1
XM_017000368.1	958	Silent Mutation	GGA,GGT	G186G	XP_016855857.1