Allele/Variant

rs794727774

Species
Homo sapiens
Symbol
rs794727774
Category
Variant
Variant type
SNP
Overlaps
FUCA1
Location
1:23848684
Nucleotide Change
C>T
Most Severe Consequence
  • stop gained
See all consequences
HGVS.g name
  • (GRCh38)1:23848684C>T
HGVS.c name
  • ENSEMBL:ENST00000374479.4:c.1125G>A
  • RefSeq:NM_000147.5:c.1125G>A
HGVS.p name
  • ENSP00000363603:p.Trp375Ter
  • NP_000138:p.Trp375Ter
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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