Variant #0000657185 (NC_000012.11:g.6777111_6777113del, NM_001039920.2:c.1194_1196del (ZNF384))

Chromosome 12
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.6777111_6777113del
DNA change (hg38) g.6667945_6667947del
Published as ZNF384(NM_001039920.2):c.1194_1196del (p.(Gln400del)), ZNF384(NM_001135734.2):c.1542_1544delGCA (p.Q516del)
ISCN -
DB-ID ZNF384_000004 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) 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF384 NM_001039920.2 -?/. - c.1194_1196del r.(?) p.(Gln400del)
ING4 NM_001127582.1 -?/. - c.-4805_-4803del r.(?) p.(=)


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