Product Details
- SNP ID
-
rs199920317
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:37850432 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGAGATGTTGCAGAACAAAGGCTTA[A/G]CAGGTATAAGGACTCCCCGGCTGTC
- Phenotype
-
MIM: 607421
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NME8
PubMed Links
Gene Details
- Gene
- NME8
- Gene Name
- NME/NM23 family member 8
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_016616.4 |
460 |
Missense Mutation |
ACA,GCA |
T30A |
NP_057700.3 |
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