Variant #0000689920 (NC_000007.13:g.128498448C>T, NM_001458.4:c.8049C>T (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.128498448C>T
DNA change (hg38) -
Published as FLNC(NM_001458.4):c.8049C>T (p.Y2683=)
ISCN -
DB-ID ATP6V1F_000016
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) 0.00046 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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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.8049C>T r.(?) p.(Tyr2683=) -
ATP6V1F NM_004231.3 -?/. - c.-4511C>T r.(?) p.(=) -


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