Variant #0000247172 (NC_000012.11:g.89891122A>G, POC1B(NM_172240.2):c.101-3T>C)

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.89891122A>G
DNA change (hg38) g.89497345A>G
Published as POC1B(NM_172240.2):c.101-3T>C
ISCN -
DB-ID POC1B_000016
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POC1B-GALNT4 NM_001199781.1 -?/. - c.*25468T>C r.(=) p.(=)
GALNT4 NM_003774.4 -?/. - c.*25468T>C r.(=) p.(=)
POC1B NM_172240.2 -?/. - c.101-3T>C r.spl? p.?