Product Details

SNP ID
rs1063155
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:122473607 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGCCATATTCTCAAATTCAAATG[C/G]CGTGATTCCAGTTGCAAATTTGCTC
Phenotype
MIM: 616381
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ZCCHC8 PubMed Links

Gene Details

Gene
ZCCHC8
Gene Name
zinc finger CCHC-type containing 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017612.4 2167 Missense Mutation CCA,GCA P672A NP_060082.2
XM_006719491.2 2167 Missense Mutation CCA,GCA P595A XP_006719554.1
XM_011538555.2 2167 Missense Mutation CCA,GCA P573A XP_011536857.1
XM_017019606.1 2167 Missense Mutation CCA,GCA P581A XP_016875095.1

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