Product Details

SNP ID
rs151311604
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:41613 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATCCTTCAAGAAGTCTTCATCATC[A/G]GGAAGGTTTGCTTCCTGAGGAGTTA
Phenotype
MIM: 611395
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM110C PubMed Links

Gene Details

Gene
FAM110C
Gene Name
family with sequence similarity 110 member C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077710.2 1222 Nonsense Mutation CGA,TGA R321* NP_001071178.2
XM_011510372.2 1222 UTR 3 XP_011508674.1
XM_017004689.1 1222 Intron XP_016860178.1
XM_017004690.1 1222 Intron XP_016860179.1
XM_017004691.1 1222 UTR 3 XP_016860180.1
XM_017004692.1 1222 Intron XP_016860181.1

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