Variant #0000248325 (NC_000019.9:g.41117869A>G, NM_001042545.1:c.2158A>G (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.41117869A>G
DNA change (hg38) g.40611963A>G
Published as LTBP4(NM_001042544.1):c.2359A>G (p.T787A)
ISCN -
DB-ID LTBP4_000035 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) 0.43959 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.2158A>G - r.(?) p.(Thr720Ala)
LTBP4 NM_003573.2 -/. - c.2248A>G - r.(?) p.(Thr750Ala)


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