Variant #0000339471 (NC_000003.11:g.150690439T>A, NM_174878.2:c.57A>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.150690439T>A
DNA change (hg38) g.150972652T>A
Published as -
ISCN -
DB-ID CLRN1_000232
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) 0.13455 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.57A>T r.(?) p.(Ala19=) -
CLRN1 NM_174878.2 -/. - c.57A>T r.(?) p.(Ala19=) -


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