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- SNP ID:
- rs10972310
- Gene
-
FANCGPIGO - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.9: 35089501 - 35089501 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TTACTTGTGAAGGAGAGGAGGAAGC[A/G]GAGCAAAAGGAGAGTTTCTATAGGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602956
MIM: 614730
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Literature Links: |
FANCG PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| FANCG - Fanconi anemia complementation group G | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| PIGO - phosphatidylinositol glycan anchor biosynthesis class O | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001201484.1 | Intron | NP_001188413.1 | ||||
| NM_032634.3 | Intron | NP_116023.2 | ||||
| NM_152850.3 | Intron | NP_690577.2 | ||||
| XM_005251619.3 | Intron | XP_005251676.1 | ||||
| XM_017015222.1 | Intron | XP_016870711.1 | ||||
| XM_017015223.1 | Intron | XP_016870712.1 | ||||
| XM_017015224.1 | Intron | XP_016870713.1 | ||||
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HapMap