Product Details
- SNP ID
-
rs147193465
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:111092380 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGCAGCTCTGGCAGAGGACTGTTC[C/T]ACTAGACACGCTGAAGGGACTGGGT
- Phenotype
-
MIM: 609669
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
WDR36
PubMed Links
Gene Details
- Gene
- WDR36
- Gene Name
- WD repeat domain 36
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_139281.2 |
209 |
Missense Mutation |
CCA,CTA |
P31L |
NP_644810.1 |
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