Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1367775137
- Species
- Homo sapiens
- Symbol
- rs1367775137
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KMT2C
- Location
- 7:152146675
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)7:152146675T>C
- HGVS.c name
- ENSEMBL:ENST00000262189.11:c.13955A>G
- ENSEMBL:ENST00000355193.1:c.14174A>G
- HGVS.p name
- ENSP00000262189:p.Gln4652Arg
- ENSP00000347325:p.Gln4725Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:152134922...152436644 (301.72 kb)
- Assembly version
- Not Available
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