Variant #0000518310 (NC_000003.11:g.150690482T>C, NM_174878.2:c.14A>G (CLRN1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.150690482T>C
DNA change (hg38) g.150972695T>C
Published as CLRN1(NM_001256819.1):c.14A>G (p.Q5R)
ISCN -
DB-ID CLRN1-AS1_000003
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 16:31:53 +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.14A>G r.(?) p.(Gln5Arg) -
CLRN1 NM_174878.2 ?/. - c.14A>G r.(?) p.(Gln5Arg) -
CLRN1-AS1 NR_024066.1 ?/. - n.18T>C r.(?) - -


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