Allele/Variant

rs371874832

Species
Homo sapiens
Symbol
rs371874832
Category
Variant
Variant type
SNP
Overlaps
ACBD7
Location
10:15078585
Nucleotide Change
G>A
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)10:15078585G>A
HGVS.c name
  • ENSEMBL:ENST00000356189.6:c.212C>T
  • ENSEMBL:ENST00000496890.1:n.376C>T
HGVS.p name
  • ENSP00000367453:p.Ala71Val
  • NP_001034933:p.Ala71Val
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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