Product Details

SNP ID
rs200290874
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:105101128 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGACTTTCAATGTATTTGGAGATGC[C/T]GGTTCAAAAACGTCATCATCATCTT
Phenotype
MIM: 604577
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
BVES PubMed Links

Gene Details

Gene
BVES
Gene Name
blood vessel epicardial substance
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199563.1 1136 Silent Mutation CCA,CCG P348P NP_001186492.1
NM_007073.4 1136 Silent Mutation CCA,CCG P348P NP_009004.2
NM_147147.3 1136 Silent Mutation CCA,CCG P348P NP_671488.1
XM_011535398.2 1136 Silent Mutation CCA,CCG P348P XP_011533700.1

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