Product Details

SNP ID
rs149706272
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:30984748 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATCTGGACCAGACAACGAACTGAG[A/C]ATCCTGGGCAAGGTAGGCTCCACTG
Phenotype
MIM: 611358
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
DPRXP4 PubMed Links

Gene Details

Gene
DPRXP4
Gene Name
divergent-paired related homeobox pseudogene 4
There are no transcripts associated with this gene.

Gene
RNF135
Gene Name
ring finger protein 135
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184992.1 826 Missense Mutation AGA,AGC R168S NP_001171921.1
NM_032322.3 826 Missense Mutation AGA,AGC R168S NP_115698.3
NM_197939.1 826 Missense Mutation AGA,AGC R168S NP_922921.1
XM_005258043.4 826 UTR 5 XP_005258100.1
XM_017025223.1 826 UTR 5 XP_016880712.1

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