Allele/Variant

rs149819971

Species
Homo sapiens
Symbol
rs149819971
Category
Variant
Variant type
SNP
Overlaps
GMDS
Location
6:1624201
Nucleotide Change
C>T
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_000006.12:g.1624201C>T
HGVS.c name
  • ENSEMBL:ENST00000380805.6:n.1349G>A
  • ENSEMBL:ENST00000380815.5:c.1087G>A
HGVS.p name
  • ENSP00000370194:p.Val363Met
  • ENSP00000436726:p.Val333Met
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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