Variant #0000808874 (NC_000019.9:g.41122881G>C, NM_001042545.1:c.2899G>C (LTBP4))

Chromosome 19
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.41122881G>C
DNA change (hg38) -
Published as LTBP4(NM_001042544.1):c.3100G>C (p.A1034P)
ISCN -
DB-ID LTBP4_000059
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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
LTBP4 NM_001042545.1 ?/. - c.2899G>C - r.(?) p.(Ala967Pro)
LTBP4 NM_003573.2 ?/. - c.2989G>C - r.(?) p.(Ala997Pro)


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