Product Details
- SNP ID
-
rs11208299
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
83
- Location
-
Chr.1:40515059 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- AGAGAGTTTCCAGTGTTTGGGGAAG[G/T]GGAGGGTGTACTTCTTGTTGGAGTG
- Phenotype
-
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
EXO5
PubMed Links
Gene Details
- Gene
- EXO5
- Gene Name
- exonuclease 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_022774.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
NP_073611.1 |
XM_005271125.3 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_005271182.1 |
XM_005271126.3 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_005271183.1 |
XM_005271128.3 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_005271185.1 |
XM_011541970.2 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_011540272.1 |
XM_017002099.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857588.1 |
XM_017002100.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857589.1 |
XM_017002101.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857590.1 |
XM_017002102.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857591.1 |
XM_017002103.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857592.1 |
XM_017002104.1 |
947 |
Missense Mutation |
GGG,GTG |
G172V |
XP_016857593.1 |
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