Allele/Variant

rs1420872103

Species
Homo sapiens
Symbol
rs1420872103
Category
Variant
Variant type
SNP
Overlaps
NUP210L
Location
1:154000927
Nucleotide Change
T>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_000001.11:g.154000927T>C
HGVS.c name
  • ENSEMBL:ENST00000271854.3:c.4931-5747A>G
  • ENSEMBL:ENST00000368553.5:c.1730-5747A>G
HGVS.p name
  • ENSP00000357547:p.Asn1772Ser
  • NP_997191:p.Asn1772Ser
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