Allele/Variant

rs754936589

Species
Homo sapiens
Symbol
rs754936589
Category
Variant
Variant type
SNP
Overlaps
RADIL
Location
7:4835062
Nucleotide Change
G>C
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)7:4835062G>C
HGVS.c name
  • ENSEMBL:ENST00000399583.4:c.961C>G
  • ENSEMBL:ENST00000445392.5:n.1079C>G
HGVS.p name
  • ENSP00000382492:p.Pro321Ala
  • NP_060529:p.Pro321Ala
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available

Genome location
Assembly version
Not Available
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Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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