Varaico: Literature-Extracted Genetic Variants

Gene:CCNQ
Variant:p.V168fs

CCNQ

28 papers

RefSeq Summary

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this ...

Pfam Domains

Cyclin_Naa 14–137UCSCCyclin, N-terminal domain
CycT2-like_Caa 150–240UCSCCyclin-T2-like, C-terminal domain

Gene Aliases

HGNC Name

cyclin Q

HGNC Previous Symbol

FAM58A

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
2 papers
NM_152274.5
p.V168fs
c.502_503fs
Surrounding Variants
2 papers
NM_152274.5
p.V168_L173Fs
c.502_518delinsAFs
1 paper
NM_152274.5
p.H179fs
c.535_536fs
1 paper
NM_152274.5
p.H179delFs
c.535delG
1 paper
NM_152274.5
p.Y148Y
c.444C>T
1 paper
NM_152274.5
p.E206*
c.616G>T
3 papers
NM_152274.5
p.W217*
c.650G>A
3 papers
NM_152274.5
p.W217*
c.651G>A
1 paper
NM_152274.5
p.Q219_V220Splc
c.657+1G>A
1 paper
NM_152274.5
p.E116_R118del0
c.346_354del9
1 paper
NM_152274.5
p.F114L
c.342C>G
2 papers
NM_152274.5
p.R113H
c.338G>A
1 paper
NM_152274.5
p.H87Y
c.259C>T
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."