Variant #0000566637 (NC_000019.9:g.18893863C>G, NC_000019.9(NM_000095.2):c.2227+1G>C (COMP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.18893863C>G
DNA change (hg38) g.18783053C>G
Published as COMP(NM_000095.2):c.2227+1G>C
ISCN -
DB-ID COMP_000138
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 2020-07-15 16:10:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMP NM_000095.2 +/. - c.2227+1G>C r.spl? p.?
CRTC1 NM_001098482.1 +/. - c.*5671C>G r.(=) p.(=)


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