Variant #0000305065 (NC_000011.9:g.66617593_66617595del, NC_000011.9(NM_001040716.1):c.2719-5_2719-3del (PC))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66617593_66617595del
DNA change (hg38) g.66850122_66850124del
Published as PC(NM_001040716.1):c.2719-5_2719-3delCTC
ISCN -
DB-ID PC_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 09:39:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PC NM_001040716.1 ?/. - c.2719-5_2719-3del r.spl? p.?
RCE1 NM_005133.2 ?/. - c.*4027_*4029del r.(=) p.(=)
LRFN4 NM_024036.4 ?/. - c.-7623_-7621del r.(?) p.(=)
C11orf80 NM_024650.3 ?/. - c.*6888_*6890del r.(=) p.(=)


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