Variant #0000676500 (NC_000002.11:g.216300405A>C, NM_212482.1:c.121T>G (FN1))

Chromosome 2
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.216300405A>C
DNA change (hg38) -
Published as FN1(NM_002026.2):c.121T>G (p.(Ser41Ala)), FN1(NM_212482.2):c.121T>G (p.S41A)
ISCN -
DB-ID FN1_000073 See all 2 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) 0.0012 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FN1 NM_212482.1 -?/. - c.121T>G r.(?) p.(Ser41Ala)


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