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- SNP ID:
- rs200785815
- Gene
-
ABCC9 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 21925308 - 21925311 on Build GRCh38
- Polymorphism:
- AGAG/-, Insertion/deletion
- Context Sequence [VIC/FAM]:
AAAAATAAAATTAGGAATATTTT[AGAG/-]AGCCTCTGATTTCCACAGAACAAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601439
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Literature Links: |
ABCC9 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| ABCC9 - ATP binding cassette subfamily C member 9 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_005691.3 | Intron | NP_005682.2 | ||||
| NM_020297.3 | Intron | NP_064693.2 | ||||
| XM_005253284.3 | Intron | XP_005253341.1 | ||||
| XM_005253286.3 | Intron | XP_005253343.1 | ||||
| XM_005253287.4 | Intron | XP_005253344.1 | ||||
| XM_005253288.3 | Intron | XP_005253345.1 | ||||
| XM_005253289.3 | Intron | XP_005253346.1 | ||||
| XM_005253290.3 | Intron | XP_005253347.1 | ||||
| XM_006719025.3 | Intron | XP_006719088.1 | ||||
| XM_011520545.2 | Intron | XP_011518847.1 | ||||
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