Product Details

SNP ID
rs12742083
Assay Type
Functionally tested
NCBI dbSNP Submissions
29
Location
Chr.1:86716765 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTAATTAGAAGTGGAAATTGGACTA[A/G]AACCGGGTGTATGAACATCCAGTCT
Phenotype
MIM: 609287
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SH3GLB1 PubMed Links

Gene Details

Gene
SH3GLB1
Gene Name
SH3 domain containing GRB2 like endophilin B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206651.1 Intron NP_001193580.1
NM_001206652.1 Intron NP_001193581.1
NM_001206653.1 Intron NP_001193582.1
NM_016009.4 Intron NP_057093.1
XM_006710672.2 Intron XP_006710735.1
XM_006710673.2 Intron XP_006710736.1
XM_011541538.1 Intron XP_011539840.1
XM_017001408.1 Intron XP_016856897.1
XM_017001409.1 Intron XP_016856898.1
XM_017001410.1 Intron XP_016856899.1

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