Variant #0000853545 (NC_000012.11:g.89853401_89853402insC, NC_000012.11(NM_172240.2):c.1113+13_1113+14insG (POC1B))

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.89853401_89853402insC
DNA change (hg38) -
Published as POC1B(NM_172240.3):c.1113+13_1113+14insG
ISCN -
DB-ID GALNT4_000015
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 -?/. - c.*63188_*63189insG r.(=) p.(=)
GALNT4 NM_003774.4 -?/. - c.*63188_*63189insG r.(=) p.(=)
POC1B NM_172240.2 -?/. - c.1113+13_1113+14insG r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.