Variant #0001004539 (NC_000019.9:g.18897410_18897412del, NM_000095.2:c.1186_1188del (COMP))

Chromosome 19
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.18897410_18897412del
DNA change (hg38) -
Published as COMP(NM_000095.2):c.1186_1188del (p.(Lys396del))
ISCN -
DB-ID COMP_000255
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMP NM_000095.2 ?/. - c.1186_1188del r.(?) p.(Lys396del)
CRTC1 NM_001098482.1 ?/. - c.*9218_*9220del r.(=) p.(=)


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