Product Details

SNP ID
rs139801882
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:7501183 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCACCTGCACGAGGACGCGCAC[A/G]CCGGGATCGGCCTCTCCAACGCGCA
Phenotype
MIM: 607583
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C19orf45 PubMed Links

Gene Details

Gene
C19orf45
Gene Name
chromosome 19 open reading frame 45
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_198534.2 502 Missense Mutation ACC,GCC T121A NP_940936.2
XM_005272473.3 502 Missense Mutation ACC,GCC T121A XP_005272530.1
XM_011527993.1 502 Missense Mutation ACC,GCC T121A XP_011526295.1
XM_011527995.2 502 Missense Mutation ACC,GCC T121A XP_011526297.1
Gene
PEX11G
Gene Name
peroxisomal biogenesis factor 11 gamma
There are no transcripts associated with this gene.

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