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- SNP ID:
- rs772001719
- Gene
-
CRYGNMIR3907 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.7: 151435949 - 151435949 on Build GRCh38
- Polymorphism:
- A/C, Transversion substitution
- Context Sequence [VIC/FAM]:
GTCTCAGGGTGCCTCTGGGGCCCAG[A/C]GTCCCTCTCTGAGGCCCTTCTGGGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609603
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Literature Links: |
CRYGN 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 |
| CRYGN - crystallin gamma N | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001308292.1 | Intron | NP_001295221.1 | ||||
| NM_144727.2 | Intron | NP_653328.1 | ||||
| XM_005249952.3 | Intron | XP_005250009.1 | ||||
| XM_011515836.1 | Intron | XP_011514138.1 | ||||
| XM_011515837.2 | Intron | XP_011514139.1 | ||||
| XM_017011773.1 | Intron | XP_016867262.1 | ||||
| MIR3907 - microRNA 3907 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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