Results for the protein: Q8N1D0

Results for the Protein: Q8N1D0

425906069

5003

SLC22A18AS

NCBI, UniProt

BWR1B_HUMAN RecName: Full=Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B protein; AltName: Full=Organic cation transporter-like protein 2 antisense protein; AltName: Full=Solute carrier family 22 member 1-like antisense protein; AltName: Full=Solute carrier family 22 member 18 antisense protein; AltName: Full=p27-Beckwith-Wiedemann region 1 B; Short=p27-BWR1B

			0 5 0 4 1

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Default View:	Swiss-Prot Protein: Q8N1D0 Identical to: NP_009036 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕

Table of Mutations found on the Protein

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
Swiss-Prot	VAR_024064	Polymorphism	p.GLY133ARG	N/A
dbSNP	rs76505120	Polymorphism	p.GLY139ARG	N/A
dbSNP	rs365605	Polymorphism	p.GLY89ASP	N/A
dbSNP	rs80153297	Polymorphism	p.GLY158GLU	N/A
dbSNP	rs114581018	Polymorphism	p.THR200PRO	N/A

Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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