Variant #0000522766 (NC_000004.11:g.57897521dup, NM_000938.1:c.*367dup (POLR2B))

Chromosome 4
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.57897521dup
DNA change (hg38) g.57031355dup
Published as IGFBP7(NM_001553.2):c.830-7dup (p.(=))
ISCN -
DB-ID IGFBP7_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
POLR2B NM_000938.1 -?/. - c.*367dup r.(?) p.(=)
IGFBP7 NM_001253835.1 -?/. - c.*1072dup r.(?) p.(=)


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