Variant #0000530890 (NC_000007.13:g.128498520T>C, NM_001458.4:c.8121T>C (FLNC))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128498520T>C
DNA change (hg38) g.128858466T>C
Published as FLNC(NM_001127487.1):c.8022T>C (p.(Ile2674=)), FLNC(NM_001458.5):c.8121T>C (p.I2707=)
ISCN -
DB-ID ATP6V1F_000006 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) 0.00935 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +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.8121T>C r.(?) p.(Ile2707=) -
ATP6V1F NM_004231.3 -/. - c.-4439T>C r.(?) p.(=) -


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