Product Details

SNP ID
rs200613398
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:100553353 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAACTATTCTTTCTCAAAGGTATGT[C/T]CCCCCAGACCAAGTCAAGGGGCCCA
Phenotype
MIM: 604019
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
AGFG2 PubMed Links

Gene Details

Gene
AGFG2
Gene Name
ArfGAP with FG repeats 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006076.4 560 Silent Mutation GTC,GTT V146V NP_006067.3
XM_005250306.2 560 Silent Mutation GTC,GTT V146V XP_005250363.1
XM_017012112.1 560 Silent Mutation GTC,GTT V59V XP_016867601.1
XM_017012113.1 560 Silent Mutation GTC,GTT V146V XP_016867602.1
XM_017012114.1 560 Intron XP_016867603.1

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