Variant #0000605122 (NC_000001.10:g.209961959C>T, NM_006147.3:c.1210G>A (IRF6))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.209961959C>T
DNA change (hg38) g.209788614C>T
Published as -
ISCN -
DB-ID C1orf74_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.1210G>A r.(?) p.(Glu404Lys)
TRAF3IP3 NM_025228.2 +/. - c.*6466C>T r.(=) p.(=)
C1orf74 NM_152485.2 +/. - c.-4312G>A r.(?) p.(=)


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