Allele/Variant

rs782637185

Species
Homo sapiens
Symbol
rs782637185
Category
Variant
Variant type
SNP
Overlaps
GLA
Location
X:101407910
Nucleotide Change
G>A
Most Severe Consequence
  • 5 prime UTR variant
See all consequences
HGVS.g name
  • (GRCh38)X:101407910G>A
HGVS.c name
  • ENSEMBL:ENST00000218516.4:c.-7C>T
  • ENSEMBL:ENST00000409170.3:c.301-4026G>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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