Variant #0000294075 (NC_000012.11:g.89864162G>A, NM_172240.2:c.786C>T (POC1B))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.89864162G>A
DNA change (hg38) g.89470385G>A
Published as POC1B(NM_172240.3):c.786C>T (p.L262=)
ISCN -
DB-ID POC1B_000005
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) 0.00163 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 -/. - c.*52428C>T r.(=) p.(=)
GALNT4 NM_003774.4 -/. - c.*52428C>T r.(=) p.(=)
POC1B NM_172240.2 -/. - c.786C>T r.(?) p.(Leu262=)


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