Varaico: Literature-Extracted Genetic Variants

Gene:RP2
Variant:p.W171delFs

RP2

369 papers

RefSeq Summary

The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubuli...

Pfam Domains

TBCCaa 59–177UCSCTubulin binding cofactor C

Gene Aliases

HGNC Name

RP2 activator of ARL3 GTPase

HGNC Alias Symbols

TBCCD2; NME10; NM23-H10

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
2 papers
NM_006915.3
p.W171delFs
c.511delT
Surrounding Variants
1 paper
NM_006915.3
p.T170I
c.509C>T
3 papers
NM_006915.3
p.W171*
c.512G>A
4 papers
NM_006915.3
p.W171*
c.513G>A
4 papers
NM_006915.3
p.S172insFs
c.515dupG
1 paper
NM_006915.3
p.S172fs
c.514_515fs
1 paper
NM_006915.3
p.S172fs
c.514_515fs
1 paper
NM_006915.3
p.N169delFs
c.507delT
5 papers
NM_006915.3
p.N173N
c.519C>T
1 paper
NM_006915.3
p.H175P
c.524A>C
1 paper
NM_006915.3
p.I166_F167delFs
c.498_499delCT
3 papers
NM_006915.3
p.F177delFs
c.530_531delTT
3 papers
NM_006915.3
p.F177fs
c.529_530fs
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