Product Details
- SNP ID
-
rs140396210
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:143060983 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGCAATCCTGCTGTCTTACTGCTCT[A/G]TCCTGTGTAACTACAAGGCCATCGA
- Phenotype
-
MIM: 608514
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
AIG1
PubMed Links
Gene Details
- Gene
- AIG1
- Gene Name
- androgen induced 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001286587.1 |
123 |
Missense Mutation |
ATC,GTC |
I10V |
NP_001273516.1 |
NM_001286588.1 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
NP_001273517.1 |
NM_001286589.1 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
NP_001273518.1 |
NM_016108.3 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
NP_057192.2 |
XM_011535881.2 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_011534183.1 |
XM_011535882.2 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_011534184.1 |
XM_011535883.2 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_011534185.1 |
XM_011535884.2 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_011534186.1 |
XM_011535885.2 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_011534187.1 |
XM_017010927.1 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_016866416.1 |
XM_017010928.1 |
123 |
Missense Mutation |
ATC,GTC |
I20V |
XP_016866417.1 |
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