Product Details

SNP ID
rs200038781
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:418975 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACGCAGGTGCAGCTCACTCTCGG[C/T]GGCCACGATGGGCTGCCCGTTCTGC
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 1582 Missense Mutation ACC,GCC T568A NP_036567.2
XM_011527893.2 1582 Intron XP_011526195.1
XM_011527894.2 1582 Intron XP_011526196.1
XM_011527895.2 1582 Missense Mutation ACC,GCC T523A XP_011526197.1
XM_011527896.2 1582 Intron XP_011526198.1
XM_017026567.1 1582 Intron XP_016882056.1

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