All variants in the BRWD3 gene

Information The variants shown are described using the NM_153252.4 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.5101G>A r.(?) p.(Gly1701Arg) - likely benign g.79932416C>T g.80676917C>T BRWD3(NM_153252.4):c.5101G>A (p.G1701R), BRWD3(NM_153252.5):c.5101G>A (p.G1701R) - BRWD3_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
-?/. - c.5101G>A r.(?) p.(Gly1701Arg) - likely benign g.79932416C>T g.80676917C>T BRWD3(NM_153252.4):c.5101G>A (p.G1701R), BRWD3(NM_153252.5):c.5101G>A (p.G1701R) - BRWD3_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.5101G>A r.(?) p.(Gly1701Arg) - likely benign g.79932416C>T g.80676917C>T BRWD3(NM_153252.4):c.5101G>A (p.G1701R), BRWD3(NM_153252.5):c.5101G>A (p.G1701R) - BRWD3_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
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