Variant #0000251208 (NC_000001.10:g.209962944A>G, NC_000001.10(NM_006147.3):c.1179+68T>C (IRF6))

Chromosome 1
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.209962944A>G
DNA change (hg38) g.209789599A>G
Published as IRF6(NM_006147.4):c.1179+68T>C
ISCN -
DB-ID IRF6_000053
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRF6 NM_006147.3 -/. - c.1179+68T>C r.(=) p.(=)
TRAF3IP3 NM_025228.2 -/. - c.*7451A>G r.(=) p.(=)
C1orf74 NM_152485.2 -/. - c.-5297T>C r.(?) p.(=)


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