Allele/Variant

rs199685737

Species
Homo sapiens
Symbol
rs199685737
Category
Variant
Variant type
SNP
Overlaps
WDR83
Location
19:12673255
Nucleotide Change
G>A
Most Severe Consequence
  • intron variant&non coding transcript variant
See all consequences
HGVS.g name
  • (GRCh38)19:12673255G>A
HGVS.c name
  • ENSEMBL:ENST00000418543.8:c.737G>A
  • ENSEMBL:ENST00000425834.7:n.426G>A
HGVS.p name
  • ENSP00000402653:p.Arg246His
  • ENSP00000449257:p.Val178Met
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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