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GGAACTTCTGGGCTTTAAAAAGACT[A/T]GCTTGAAAGCCTGTGCTGAAGTAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615912 MIM: 611355 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GSTCD PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GSTCD - glutathione S-transferase C-terminal domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031720.3 | 484 | Missense Mutation | AGC,TGC | S,C 136 | NP_001026890.2 | |
NM_024751.3 | 484 | Intron | NP_079027.2 | |||
XM_005263222.3 | 484 | Missense Mutation | AGC,TGC | S,C 136 | XP_005263279.1 | |
XM_011532248.2 | 484 | Missense Mutation | AGC,TGC | S,C 136 | XP_011530550.1 | |
XM_011532249.2 | 484 | Missense Mutation | AGC,TGC | S,C 136 | XP_011530551.1 | |
XM_011532252.2 | 484 | Missense Mutation | AGC,TGC | S,C 136 | XP_011530554.1 |
INTS12 - integrator complex subunit 12 | ||||||
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There are no transcripts associated with this gene. |