Variant #0001042968 (NC_000019.9:g.41117300G>A, NM_001042545.1:c.2053G>A (LTBP4))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41117300G>A
DNA change (hg38) -
Published as LTBP4(NM_003573.2):c.2143G>A (p.D715N)
ISCN -
DB-ID LTBP4_000042 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) 0.0078 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
LTBP4 NM_001042545.1 -/. - c.2053G>A - r.(?) p.(Asp685Asn)
LTBP4 NM_003573.2 -/. - c.2143G>A - r.(?) p.(Asp715Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.