All transcript variants in gene APTX

Information The variants shown are described using the NM_175073.2 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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.484-25_484-4del likely benign r.spl? p.? g.32986041_32986062del - APTX(NM_001195249.1):c.484-25_484-4delGTTTTTTTTTTTGTTTTTTTTT - APTX_000071 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-/. - c.484-25_484-4del benign r.spl? p.? g.32986041_32986062del - APTX(NM_001195249.1):c.484-25_484-4delGTTTTTTTTTTTGTTTTTTTTT - APTX_000071 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.484-25_484-4del benign r.spl? p.? g.32986041_32986062del - APTX(NM_001195249.1):c.484-25_484-4delGTTTTTTTTTTTGTTTTTTTTT - APTX_000071 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
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