All variants in the EPCAM gene


NOTE: alias for geneID is TACSTD1
Information The variants shown are described using the NM_002354.2 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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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     
+/. 7i_9_ c.859-689_*14697del r.? p.? - pathogenic (dominant) g.47611616_47628449del g.47384477_47401311del - - EPCAM_000082 16834 bp deletion C_AluSx1 to C_AluSx1 Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. PubMed: Kuiper 2011 - - Germline - - - 0 - Mamata Sivagnanam
+/. 7i_9_ c.859-689_*14697del r.? p.? - pathogenic (dominant) g.47611616_47628449del g.47384477_47401311del - - EPCAM_000082 16834 bp deletion C_AluSx1 to C_AluSx1 Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. PubMed: Kuiper 2011 - - Germline - - - 0 - Mamata Sivagnanam
+/. 7i_9_ c.859-689_*14697del r.? p.? - pathogenic (dominant) g.47611616_47628449del g.47384477_47401311del - - EPCAM_000082 16834 bp deletion C_AluSx1 to C_AluSx1 Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. PubMed: Kuiper 2011 - - Germline - - - 0 - Mamata Sivagnanam
+/. 7i_9_ c.859-689_*14697del r.? p.? - pathogenic (dominant) g.47611616_47628449del g.47384477_47401311del - - EPCAM_000082 16834 bp deletion C_AluSx1 to C_AluSx1 Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. PubMed: Spaepen 2013 - - Germline - - - 0 - Mamata Sivagnanam
+/. 7i_9_ c.859-689_*14697del r.? p.? - pathogenic (dominant) g.47611616_47628449del g.47384477_47401311del AC079775.6:g.79465_96299del16834 - EPCAM_000082 16834 bp deletion C_AluSx1 to C_AluSx1 Variant Error [EBUILDMISMATCH]: This variant seems to mismatch; the genomic variants on hg19 and hg38 seem to not belong together. Please fix this entry and then remove this message. PubMed: Van der Klift 2005 - - Germline - - - 0 - Mamata Sivagnanam
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