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TGCTGCCCCCGCCGGCCGCACTCGC[A/C]GTGCTGGCCGCCGCCGGCTGGATCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607028 MIM: 614232 | ||||||||||||||||||||
Literature Links: |
ATP6V0D1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ATP6V0D1 - ATPase H+ transporting V0 subunit d1 | ||||||
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There are no transcripts associated with this gene. |
HSD11B2 - hydroxysteroid 11-beta dehydrogenase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000196.3 | 293 | Silent Mutation | GCA,GCC | A,A 59 | NP_000187.3 |