Product Details

SNP ID
rs201239038
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:30025732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCCCATGCTCACTCACCTGGAT[A/G]AGGATCTTGCCAAGGCAGACGAAGG
Phenotype
MIM: 604567 MIM: 615175
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C16orf92 PubMed Links

Gene Details

Gene
C16orf92
Gene Name
chromosome 16 open reading frame 92
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001109659.1 1173 Intron NP_001103129.1
NM_001109660.1 1173 Intron NP_001103130.1
Gene
DOC2A
Gene Name
double C2 domain alpha
There are no transcripts associated with this gene.

Gene
FAM57B
Gene Name
family with sequence similarity 57 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318504.1 1173 Silent Mutation CTC,CTT L128L NP_001305433.1
NM_031478.5 1173 Silent Mutation CTC,CTT L178L NP_113666.2
XM_005255613.3 1173 Silent Mutation CTC,CTT L178L XP_005255670.1
XM_005255614.3 1173 Silent Mutation CTC,CTT L178L XP_005255671.1
XM_005255615.2 1173 Silent Mutation CTC,CTT L178L XP_005255672.1
XM_017023749.1 1173 Silent Mutation CTC,CTT L264L XP_016879238.1
XM_017023750.1 1173 Silent Mutation CTC,CTT L178L XP_016879239.1
XM_017023751.1 1173 Silent Mutation CTC,CTT L178L XP_016879240.1
XM_017023752.1 1173 Silent Mutation CTC,CTT L178L XP_016879241.1
XM_017023753.1 1173 Silent Mutation CTC,CTT L128L XP_016879242.1
XM_017023754.1 1173 Silent Mutation CTC,CTT L128L XP_016879243.1

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