Full data view for gene DCC

Information The variants shown are described using the NM_005215.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 15 c.2227A>T r.(?) p.(Met743Leu) FN3-4 Unknown ACMG likely pathogenic g.50866145A>T g.53339775A>T - - DCC_000023 {CV:375285} ACMG: PM1, PP4, BS1, BP4 - Likely benign Journal: Marsh 2017 - rs199651452 Germline - - - - - DNA SEQ Blood - ? - Journal: Marsh 2017 - M - France white - - - - 1 Ashley Marsh
+?/. 15 c.2227A>T r.(?) p.(Met743Leu) FN3-4 Paternal (confirmed) - likely pathogenic g.50866145A>T g.53339775A>T - - DCC_000023 {CV:375285} Journal: Marsh 2017 - rs199651452 Germline - - - - - DNA SEQ Blood - ACC - Journal: Marsh 2017 - M - France white - - - - 1 Ashley Marsh
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