Variant #0000544989 (NC_000011.9:g.65319803T>G, NM_001130144.2:c.1261A>C (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.65319803T>G
DNA change (hg38) g.65552332T>G
Published as LTBP3(NM_001130144.2):c.1261A>C (p.T421P)
ISCN -
DB-ID LTBP3_000030
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 ?/. - c.1261A>C r.(?) p.(Thr421Pro)
SCYL1 NM_020680.3 ?/. - c.*13766T>G r.(=) p.(=)


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