Variant #0000605121 (NC_000001.10:g.209961851A>G, NM_006147.3:c.1318T>C (IRF6))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.209961851A>G
DNA change (hg38) g.209788506A>G
Published as IRF6(NM_001206696.1):c.1033T>C (p.(Tyr345His))
ISCN -
DB-ID C1orf74_000003
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 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRF6 NM_006147.3 ?/. - c.1318T>C r.(?) p.(Tyr440His)
TRAF3IP3 NM_025228.2 ?/. - c.*6358A>G r.(=) p.(=)
C1orf74 NM_152485.2 ?/. - c.-4204T>C r.(?) p.(=)


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