Allele/Variant

rs9480941

Species
Homo sapiens
Symbol
rs9480941
Category
Variant
Variant type
SNP
Overlaps
CD164
Location
6:109370436
Nucleotide Change
T>C
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000006.12:g.109370436T>C
HGVS.c name
  • ENSEMBL:ENST00000275080.11:c.363A>G
  • ENSEMBL:ENST00000310786.10:c.402A>G
HGVS.p name
  • ENSP00000275080:p.Thr121=
  • ENSP00000309376:p.Thr134=
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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