Variant #0000544986 (NC_000011.9:g.65315000_65315008del, NM_001130144.2:c.2014_2022del (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.65315000_65315008del
DNA change (hg38) g.65547529_65547537del
Published as LTBP3(NM_001130144.2):c.2014_2022delGACGGCGGC (p.D672_G674del)
ISCN -
DB-ID LTBP3_000027
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 2019-07-18 18:22:55 +02:00 (CEST)
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.2014_2022del r.(?) p.(Asp672_Gly674del)
SCYL1 NM_020680.3 ?/. - c.*8963_*8971del r.(=) p.(=)


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