Product Details

SNP ID
rs201942283
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:16519231 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTGTTCCTGCGGTAGTTCTCATA[C/G]GGGTCATCCAGAGCCACGCCCACGC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
C19orf44 PubMed Links

Gene Details

Gene
C19orf44
Gene Name
chromosome 19 open reading frame 44
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288834.1 2753 Intron NP_001275763.1
NM_032207.3 2753 Intron NP_115583.1
XM_006722920.3 2753 Intron XP_006722983.1
XM_011528354.2 2753 Intron XP_011526656.1
XM_017027350.1 2753 Intron XP_016882839.1
Gene
CHERP
Gene Name
calcium homeostasis endoplasmic reticulum protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006387.5 2753 Silent Mutation CCC,CCG P893P NP_006378.3

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