Product Details

SNP ID
rs116126071
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:10859934 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCAGAGATCGAGAATCCTGCTGG[C/G]CCCAGATTAACTTCGACAGCACAGG
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C19orf38 PubMed Links

Gene Details

Gene
C19orf38
Gene Name
chromosome 19 open reading frame 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136482.1 906 Missense Mutation CCC,GCC P161A NP_001129954.1
XM_005259846.4 906 Missense Mutation CCC,GCC P161A XP_005259903.1
XM_005259847.4 906 Missense Mutation CCC,GCC P161A XP_005259904.1

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