Variant #0000349438 (NC_000012.11:g.89860653del, NM_172240.2:c.927del (POC1B))

Chromosome 12
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.89860653del
DNA change (hg38) g.89466876del
Published as -
ISCN -
DB-ID POC1B_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-02 17:38:44 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 +/. - c.*55938del r.(?) p.(=)
GALNT4 NM_003774.4 +/. - c.*55938del r.(?) p.(=)
POC1B NM_172240.2 +/. - c.927del r.(?) p.(Thr310ProfsTer34)


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