Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs569622614
- Species
- Homo sapiens
- Symbol
- rs569622614
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RUNX1T1
- Location
- 8:91970768
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000008.11:g.91970768C>T
- HGVS.c name
- ENSEMBL:ENST00000265814.4:c.1429G>A
- ENSEMBL:ENST00000360348.6:c.1318G>A
- HGVS.p name
- ENSP00000265814:p.Asp477Asn
- ENSP00000353504:p.Asp440Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:91954967...92103385 (148.42 kb)
- Assembly version
- Not Available
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