Product Details
- SNP ID
-
rs61740725
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:23703059 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCACCCTGGTCCCGCCGCCGAGGG[G/T]CGAGGCCGCGTTCAGGCCGGGCTCT
- Phenotype
-
MIM: 611770
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NKX2-6
PubMed Links
Gene Details
- Gene
- NKX2-6
- Gene Name
- NK2 homeobox 6
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001136271.2 |
298 |
Missense Mutation |
ACC,CCC |
T100P |
NP_001129743.2 |
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