Variant #0000613556 (NC_000011.9:g.65325348_65325356dup, NM_001130144.2:c.97_105dup (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.65325348_65325356dup
DNA change (hg38) g.65557877_65557885dup
Published as LTBP3(NM_001130144.2):c.97_105dupCTGCTGCTG (p.L33_L35dup), LTBP3(NM_001130144.3):c.97_105dupCTGCTGCTG (p.L33_L35dup)
ISCN -
DB-ID LTBP3_000055 See all 4 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.97_105dup r.(?) p.(Leu33_Leu35dup)
SCYL1 NM_020680.3 -?/. - c.*19311_*19319dup r.(=) p.(=)


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