Full data view for gene DSC2

Information The variants shown are described using the NM_004949.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/? 16 c.2686_2687dup r.(?) p.(Ala897Lysfs*3) Cytoplasmic Unknown - pathogenic g.28648046_28648047dup - 2687_2688insGA - DSC2_000031 Variant Error [EMISMATCH/ERANGE]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: van Tintelen, PubMed: Bhuiyan, ARVD/C database 7536 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: van Tintelen, PubMed: Bhuiyan - - - - - - - - - 5 Paul van der Zwaag
?/? 16 c.2686_2687dup r.(?) p.(Ala897Lysfs*3) Cytoplasmic Unknown - VUS g.28648046_28648047dup - 2687_2688insGA - DSC2_000031 Variant Error [EMISMATCH/ERANGE]: This transcript variant has an error. Please fix this entry and then remove this message. unpublished, ARVD/C database 7536 - - Germline - - - - - DNA SEQ - - ? - - - - - - - - - - - 1 Paul van der Zwaag
+/? 16 c.2686_2687dup r.(?) p.(Ala897Lysfs*3) Cytoplasmic Unknown - pathogenic g.28648046_28648047dup - 2687_2688insGA - DSC2_000031 Variant Error [EMISMATCH/ERANGE]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: De Bortoli, ARVD/C database 7536 - - Germline - - - - - DNA SEQ - - ARVD/C - PubMed: De Bortoli 4 out of 5 patients carried one or two mutations in different ARVC/D genes (De Bortoli et al.) - - - - - - - - 1 Paul van der Zwaag
-/? 16 c.2686_2687dup r.(?) p.(Ala897Lysfs*3) Cytoplasmic Unknown - benign g.28648046_28648047dup - 2687_2688insGA - DSC2_000031 Variant Error [EMISMATCH/ERANGE]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: den Haan, ARVD/C database 7536 - - Germline - - - - - DNA SEQ - - ? - PubMed: den Haan - - - - - - - - - 1 Paul van der Zwaag
+/? 16 c.2686_2687dup r.(?) p.(Ala897Lysfs*3) Cytoplasmic Unknown - pathogenic g.28648046_28648047dup - 2687_2688insGA - DSC2_000031 Variant Error [EMISMATCH/ERANGE]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Syrris et al. - - Germline - - - - - DNA SEQ - - ? - PubMed: Syrris et al. - - - - - - - - - 1 Paul van der Zwaag
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