Allele/Variant

rs375406465

Species
Homo sapiens
Symbol
rs375406465
Category
Variant
Variant type
SNP
Overlaps
MTO1
Location
6:73461810
Nucleotide Change
C>A
Most Severe Consequence
  • 5 prime UTR variant
See all consequences
HGVS.g name
  • NC_000006.12:g.73461810C>A
HGVS.c name
  • ENSEMBL:ENST00000370300.8:c.-45C>A
  • ENSEMBL:ENST00000370305.5:c.-6+16C>A
HGVS.p name
Not Available
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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