Variant #0000530893 (NC_000007.13:g.128498652_128498653dup, NM_001458.4:c.*75_*76dup (FLNC))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128498652_128498653dup
DNA change (hg38) g.128858598_128858599dup
Published as FLNC(NM_001458.4):c.*74_*75dupAC
ISCN -
DB-ID ATP6V1F_000008
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
FLNC NM_001458.4 -?/. - c.*75_*76dup r.(=) p.(=) -
ATP6V1F NM_004231.3 -?/. - c.-4307_-4306dup r.(?) p.(=) -


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