Product Details
- SNP ID
-
rs139177513
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:5916902 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTCCACCCATCACCCCTGAGTGCC[A/G]CCAAGTCCTGAAGACGAGTAAGTGT
- Phenotype
-
MIM: 118920
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CHGB
PubMed Links
Gene Details
- Gene
- CHGB
- Gene Name
- chromogranin B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001819.2 |
479 |
Missense Mutation |
CAC,CGC |
H58R |
NP_001810.2 |
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