Variant #0000622676 (NC_000011.9:g.65325342_65325356dup, NM_001130144.2:c.91_105dup (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.65325342_65325356dup
DNA change (hg38) g.65557871_65557885dup
Published as LTBP3(NM_001130144.2):c.91_105dupCTGCTGCTGCTGCTG (p.L31_L35dup)
ISCN -
DB-ID LTBP3_000054
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 ?/. - c.91_105dup r.(?) p.(Leu31_Leu35dup)
SCYL1 NM_020680.3 ?/. - c.*19305_*19319dup r.(=) p.(=)


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