Variant #0000679263 (NC_000011.9:g.65305564C>T, NM_001130144.2:c.*987G>A (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.65305564C>T
DNA change (hg38) -
Published as SCYL1(NM_020680.3):c.2158C>T (p.R720W), SCYL1(NM_020680.4):c.2158C>T (p.(Arg720Trp))
ISCN -
DB-ID LTBP3_000015 See all 2 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) 0.00252 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.*987G>A r.(=) p.(=)
SCYL1 NM_020680.3 ?/. - c.2158C>T r.(?) p.(Arg720Trp)


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