Allele/Variant

rs559815627

Species
Homo sapiens
Symbol
rs559815627
Category
Variant
Variant type
SNP
Overlaps
ATRAID
Location
2:27212331
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCh38)2:27212331C>T
HGVS.c name
  • ENSEMBL:ENST00000380171.9:c.-38C>T
  • ENSEMBL:ENST00000428518.5:c.-335+132G>A
HGVS.p name
  • ENSP00000484228:p.Pro43Leu
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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