Allele/Variant

rs757259526

Species
Homo sapiens
Symbol
rs757259526
Category
Variant
Variant type
SNP
Overlaps
NUP210L
Location
1:154154957
Nucleotide Change
C>T
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)1:154154957C>T
HGVS.c name
  • ENSEMBL:ENST00000271854.3:c.88G>A
  • ENSEMBL:ENST00000368559.8:c.88G>A
HGVS.p name
  • ENSP00000271854:p.Val30Ile
  • ENSP00000357547:p.Val30Ile
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available

Genome location
Assembly version
Not Available
Viewer Help
154.00M154.02M154.04M154.06M154.08M154.10M154.12M154.14M

Variant Molecular Consequences