Unique variants in the RAB24 gene

Information The variants shown are described using the NM_130781.2 transcript reference sequence.

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

Reported     

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     
-?/. 1 - c.-3761T>C r.(?) p.(=) - likely benign g.176734136A>G - MXD3(NM_001142935.1):c.566T>C (p.(Ile189Thr)) - MXD3_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-?/. 1 - c.265+4A>G r.spl? p.? - likely benign g.176729749T>C g.177302748T>C RAB24(NM_001031677.2):c.265+4A>G (p.?) - NSD1_000231 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-?/. 1 - c.265+14_265+16del r.(=) p.(=) - likely benign g.176729746_176729748del - RAB24(NM_001031677.2):c.265+14_265+16del (p.(=)) - NSD1_000455 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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