Variant #0000327018 (NC_000002.11:g.58386930_58386933dup, NM_018062.3:c.1096_1099dup (FANCL))

Chromosome 2
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.58386930_58386933dup
DNA change (hg38) g.58159795_58159798dup
Published as FANCL(NM_001114636.1):c.1111_1114dup (p.(Thr372Asnfs*13)), FANCL(NM_001114636.1):c.1111_1114dupATTA (p.T372Nfs*13)
ISCN -
DB-ID FANCL_000003 See all 14 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
VRK2 NM_006296.5 ?/. - c.*102_*105dup r.(=) p.(=) -
FANCL NM_018062.3 ?/. - c.1096_1099dup r.(?) p.(Thr367AsnfsTer13) -


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