Allele/Variant

rs758601966

Species
Homo sapiens
Symbol
rs758601966
Category
Variant
Variant type
SNP
Overlaps
KIAA0825
Location
5:94537026
Nucleotide Change
A>G
Most Severe Consequence
  • missense variant
See all consequences
HGVS.g name
  • (GRCh38)5:94537026A>G
HGVS.c name
  • ENSEMBL:ENST00000329378.7:c.101T>C
  • ENSEMBL:ENST00000513200.7:c.101T>C
HGVS.p name
  • ENSP00000331385:p.Ile34Thr
  • ENSP00000424618:p.Ile34Thr
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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