Full data view for gene CRLF1

Information The variants shown are described using the NM_004750.4 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     
+/. _1_1i c.(?_-1)_(115+1_116-1)del r.0? p.0? - Parent #1 - pathogenic g.18717352_18717466del - - - CRLF1_000013 Variant Error [EMISMATCH/EUNCERTAIN]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Thomas 2008 - - Unknown ? - - - - DNA SEQ - - CISS - PubMed: Thomas 2008 - M ? India - - - - - 1 Insa Buers
+/. _1_1i c.(?_-1)_(115+1_116-1)del r.0? p.0? - Parent #2 - pathogenic g.18717352_18717466del - - - CRLF1_000013 Variant Error [EMISMATCH/EUNCERTAIN]: This transcript variant has an error. Please fix this entry and then remove this message. PubMed: Thomas 2008 - - Unknown ? - - - - DNA SEQ - - CISS - PubMed: Thomas 2008 - M ? India - - - - - 1 Insa Buers
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