Allele/Variant

rs690016551

Species
Homo sapiens
Symbol
rs690016551
Category
Variant
Variant type
SNP
Overlaps
CSF1R
Location
5:150056039
Nucleotide Change
C>G
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • NC_000005.10:g.150056039C>G
HGVS.c name
  • ENSEMBL:ENST00000286301.7:c.2541G>C
  • ENSEMBL:ENST00000504875.5:n.2541G>C
HGVS.p name
  • ENSP00000286301:p.Glu847Asp
  • ENSP00000501699:p.Glu847Asp
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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