Product Details

SNP ID
rs202025962
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:13913249 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCTATCAGACAGCAATTGAAAGC[A/G]CCAGACAAGCTGGAGACAGCGCCAA
Phenotype
MIM: 610055
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C19orf57 PubMed Links

Gene Details

Gene
C19orf57
Gene Name
chromosome 19 open reading frame 57
There are no transcripts associated with this gene.

Gene
CC2D1A
Gene Name
coiled-coil and C2 domain containing 1A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017721.4 759 Missense Mutation ACC,GCC T154A NP_060191.3
XM_005259972.2 759 Missense Mutation ACC,GCC T154A XP_005260029.1
XM_005259973.2 759 Missense Mutation ACC,GCC T154A XP_005260030.1
XM_005259974.2 759 Missense Mutation ACC,GCC T154A XP_005260031.1
XM_005259975.2 759 Missense Mutation ACC,GCC T154A XP_005260032.1

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