Product Details

SNP ID
rs13194610
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:117270592 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCAGCTTCCCCGCCTCCTTCTGGAA[C/T]AGCGCGTACCAGGCGCCAGTGCCCC
Phenotype
MIM: 609979
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
VGLL2 PubMed Links

Gene Details

Gene
VGLL2
Gene Name
vestigial like family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153453.1 464 Intron NP_703154.1
NM_182645.3 464 Silent Mutation AAC,AAT N147N NP_872586.1
XM_005266883.2 464 Silent Mutation AAC,AAT N147N XP_005266940.1

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