Variant #0000518306 (NC_000003.11:g.150658308T>A, NC_000003.11(NM_174878.2):c.433+1061A>T (CLRN1))

Chromosome 3
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.150658308T>A
DNA change (hg38) g.150940521T>A
Published as CLRN1(NM_001256819.2):c.*47+1061A>T
ISCN -
DB-ID CLRN1_000227 See all 3 reported entries
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) 0.00049 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 16:31:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CLRN1 NM_001195794.1 -/. - c.434-2A>T r.spl? p.? -
CLRN1 NM_174878.2 -/. - c.433+1061A>T r.(=) p.(=) -


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