Varaico: Literature-Extracted Genetic Variants

Gene:SLFN14
Variant:p.F155L

SLFN14

74 papers

RefSeq Summary

The protein encoded by this gene plays an important role in platelet formation and function. Defects in this gene are a cause of thrombocytopenia with excessive bleeding. [provided by RefSeq, Jul 2016...

Pfam Domains

B3Raa 83–204UCSCPoxviridae B3 protein
SLFN_AlbA_2aa 206–340UCSCSchlafen, AlbA_2
SLFN_GTPase-likeaa 400–535UCSCSchlafen, GTPase-like domain

Gene Aliases

HGNC Name

schlafen family member 14

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_001129820.2
p.F155L
c.465T>A
Surrounding Variants
1 paper
NM_001129820.2
p.F155L
c.465T>G
1 paper
NM_001129820.2
p.F155L
c.463T>C
3 papers
NM_001129820.2
p.V172A
c.515T>C
1 paper
NM_001129820.2
p.R133K
c.398G>A
1 paper
NM_001129820.2
p.D115A
c.344A>C
1 paper
NM_001129820.2
p.E206Q
c.616G>C
2 papers
NM_001129820.2
p.E206A
c.617A>C
1 paper
NM_001129820.2
p.E211Q
c.631G>C
2 papers
NM_001129820.2
p.E211A
c.632A>C
1 paper
NM_001129820.2
p.K213R
c.638A>G
20 papers
NM_001129820.2
p.K218E
c.652A>G
1 paper
NM_001129820.2
p.Q93R
c.278A>G
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