Variant #0000267941 (NC_000005.9:g.176831186del, NC_000005.9(NM_000505.3):c.1018+19del (F12))

Chromosome 5
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.176831186del
DNA change (hg38) g.177404185del
Published as F12(NM_000505.4):c.1018+19delG
ISCN -
DB-ID F12_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
F12 NM_000505.3 -/. - c.1018+19del r.(=) p.(=)
PFN3 NM_001029886.2 -/. - c.-3601del r.(?) p.(=)


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