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- SNP ID:
- rs192571038
- Gene
-
ALKBH7GTF2F1MIR6885PSPN - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.19: 6380353 - 6380353 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
CGGGGTTGAGTCGCTTGAGGATCTG[C/G]GCCAACACGTTCACTGTCTGCTCGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613305
MIM: 189968
MIM: 602921
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Literature Links: |
ALKBH7 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
|
| ALKBH7 - alkB homolog 7 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| GTF2F1 - general transcription factor IIF subunit 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_002096.2 | 1767 | Silent Mutation | GCC,GCG | A,A 494 | NP_002087.2 | |
| MIR6885 - microRNA 6885 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| PSPN - persephin | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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