Varaico: Literature-Extracted Genetic Variants

Gene:HAP1
Variant:p.W104L

HAP1

233 papers

RefSeq Summary

Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a ...

Gene Aliases

HGNC Name

huntingtin associated protein 1

HGNC Previous Symbol

HAP2

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_177977.3
p.W104L
c.311G>T
Surrounding Variants
1 paper
NM_177977.3
p.W104S
c.311G>C
3 papers
NM_177977.3
p.W104*
c.311G>A
2 papers
NM_177977.3
p.W104*
c.312G>A
1 paper
NM_177977.3
p.T105S
c.313A>T
1 paper
NM_177977.3
p.T105A
c.313A>G
1 paper
NM_177977.3
p.T105P
c.313A>C
2 papers
NM_177977.3
p.P103L
c.308C>T
1 paper
NM_177977.3
p.T105I
c.314C>T
1 paper
NM_177977.3
p.T105S
c.314C>G
1 paper
NM_177977.3
p.P103R
c.308C>G
1 paper
NM_177977.3
p.T105N
c.314C>A
1 paper
NM_177977.3
p.P103Q
c.308C>A
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