All transcript variants in gene APTX

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

4 entries on 1 page. Showing entries 1 - 4.
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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     
-/- 7i c.771-12dup benign r.(?) p.? g.32974571dup - 771-12dupT - APTX_000033 - - - - Germline - - - 0 - Rick van Minkelen
-?/. - c.771-12dup likely benign r.(=) p.(=) g.32974579dup - APTX(NM_001195249.1):c.771-12dupT - APTX_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
-/. - c.771-12dup benign r.(=) p.(=) g.32974579dup - APTX(NM_001195249.1):c.771-12dupT - APTX_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-/. - c.771-12dup benign r.(=) p.(=) g.32974579dup - APTX(NM_001195249.1):c.771-12dupT - APTX_000033 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
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