Version: 8.0.0
Date: Tue Jan 28 2025
rs1559134483
Variant overlaps ABCA12
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs1559134483

Species
Homo sapiens
Symbol
rs1559134483
Category
Variant
Variant type
SNP
Overlaps
ABCA12
Location
2:214991035
Nucleotide Change
T>C
Most Severe Consequence
  • splice region variant&intron variant
See all consequences
HGVS.g name
  • NC_000002.12:g.214991035T>C
HGVS.c name
  • ENSEMBL:ENST00000272895.12:c.3295-4A>G
  • ENSEMBL:ENST00000389661.4:c.2341-4A>G
HGVS.p name
Not Available
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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