Variant #0000017970 (NC_000002.11:g.75897424_75897429del, NC_000002.11(NM_003203.4):c.1957-19_1957-14del (GCFC2))

Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.75897424_75897429del
DNA change (hg38) g.75670298_75670303del
Published as delTCAAGT
ISCN -
DB-ID GCFC2_000001
Variant remarks variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me.
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00328 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-06 09:56:35 +02:00 (CEST)
Date last edited 2014-06-18 15:15:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCFC2 NM_003203.4 ?/? ?i c.1957-19_1957-14del r.(=) p.(=)


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