Variant #0000545000 (NC_000011.9:g.65325357G>A, NM_001130144.2:c.74C>T (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.65325357G>A
DNA change (hg38) g.65557886G>A
Published as LTBP3(NM_001130144.2):c.74C>T (p.(Ala25Val))
ISCN -
DB-ID LTBP3_000040
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 -?/. - c.74C>T r.(?) p.(Ala25Val)
SCYL1 NM_020680.3 -?/. - c.*19320G>A r.(=) p.(=)


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