Product Details
- SNP ID
-
rs5658
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:129975838 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CGCGATGCCCGGCCCTTGGTTGCTG[G/C]TCGCTCTGGCTTTGACCCTGAACCT
- Phenotype
-
MIM: 613879
- Polymorphism
- G/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
TRH
PubMed Links
Gene Details
- Gene
- TRH
- Gene Name
- thyrotropin releasing hormone
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_007117.4 |
461 |
Missense Mutation |
CTC,GTC |
L8V |
NP_009048.1 |
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