Product Details
- SNP ID
-
rs138090483
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
1
- Location
-
Chr.1:164563302 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTTTAATGTGTTGTGTGAAATCAAA[A/G]AAAAAACAGGTAGGAATGAGATTCC
- Phenotype
-
MIM: 176310
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PBX1
PubMed Links
Gene Details
- Gene
- PBX1
- Gene Name
- PBX homeobox 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001204961.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
NP_001191890.1 |
NM_001204963.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
NP_001191892.1 |
NM_002585.3 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
NP_002576.1 |
XM_005245228.3 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_005245285.1 |
XM_005245229.3 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_005245286.1 |
XM_011509590.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_011507892.1 |
XM_011509591.2 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_011507893.1 |
XM_011509592.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_011507894.1 |
XM_017001395.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_016856884.1 |
XM_017001396.1 |
719 |
Missense Mutation |
AAA,GAA |
K86E |
XP_016856885.1 |
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