Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1368315881
- Species
- Homo sapiens
- Symbol
- rs1368315881
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NHSL1
- Location
- 6:138424749
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:138424749G>T
- HGVS.c name
- ENSEMBL:ENST00000343505.10:c.4153C>A
- ENSEMBL:ENST00000427025.6:c.4165C>A
- HGVS.p name
- ENSP00000344672:p.Pro1385Thr
- ENSP00000394546:p.Pro1389Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:138422043...138693212 (271.17 kb)
- Assembly version
- Not Available
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