Variant #0000860644 (NC_000007.13:g.128498517C>T, NM_001458.4:c.8118C>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.128498517C>T
DNA change (hg38) -
Published as FLNC(NM_001127487.1):c.8019C>T (p.(Leu2673=)), FLNC(NM_001458.5):c.8118C>T (p.L2706=)
ISCN -
DB-ID FLNC_000142 See all 3 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) 0.00951 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.8118C>T r.(?) p.(Leu2706=) -
ATP6V1F NM_004231.3 -?/. - c.-4442C>T r.(?) p.(=) -


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