Product Details
- SNP ID
-
rs199576209
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:37850283 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGTAGATAAATGGCAAGCAAAAAAC[A/G]AGAAGTCCAGTTACAGGTGGGTCTG
- 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 |
389 |
Missense Mutation |
CAA,CGA |
Q6R |
NP_057700.3 |
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