Variant #0000917029 (NC_000003.11:g.150690352A>C, NM_174878.2:c.144T>G (CLRN1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.150690352A>C
DNA change (hg38) g.150972565A>C
Published as -
ISCN -
DB-ID CLRN1_000007 See all 100 reported entries
Variant remarks PS3_M, PM3_VS
Reference -
ClinVar ID -
dbSNP ID rs111033258
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00026 View details
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-01-17 17:47:01 +01:00 (CET)
Date last edited 2023-01-17 17:48:45 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CLRN1 NM_174878.2 +?/+? 01 c.144T>G r.(?) p.(Asn48Lys) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.