Variant #0000979734 (NC_000011.9:g.65299084_65299086del, NM_001130144.2:c.*7468_*7470del (LTBP3))

Chromosome 11
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.65299084_65299086del
DNA change (hg38) -
Published as SCYL1(NM_020680.4):c.1046_1048del (p.(Lys349del))
ISCN -
DB-ID SCYL1_000048
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 ?/. - c.*7468_*7470del r.(=) p.(=)
SCYL1 NM_020680.3 ?/. - c.1046_1048del r.(?) p.(Lys349del)


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