Product Details

SNP ID
rs202015616
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:418938 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCACACACCTGGCTCAGGGCTCC[C/T]GTGAGACCACGCCACGCAGGTGCAG
Phenotype
MIM: 610336 MIM: 605217
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C2CD4C PubMed Links

Gene Details

Gene
C2CD4C
Gene Name
C2 calcium dependent domain containing 4C
There are no transcripts associated with this gene.

Gene
SHC2
Gene Name
SHC adaptor protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012435.2 1619 Missense Mutation CAG,CGG Q580R NP_036567.2
XM_011527893.2 1619 Intron XP_011526195.1
XM_011527894.2 1619 Intron XP_011526196.1
XM_011527895.2 1619 Missense Mutation CAG,CGG Q535R XP_011526197.1
XM_011527896.2 1619 Intron XP_011526198.1
XM_017026567.1 1619 Intron XP_016882056.1

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