Variant #0000925471 (NC_000011.9:g.65307871_65307879dup, NC_000011.9(NM_001130144.2):c.3107-23_3107-15dup (LTBP3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65307871_65307879dup
DNA change (hg38) -
Published as LTBP3(NM_001130144.3):c.3107-23_3107-15dupACCCACGCT
ISCN -
DB-ID SCYL1_000023
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +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.3107-23_3107-15dup r.(=) p.(=)
SCYL1 NM_020680.3 -?/. - c.*1834_*1842dup r.(=) p.(=)


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