Variant #0000326510 (NC_000019.9:g.41133005G>A, NM_001042545.1:c.4111G>A (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.41133005G>A
DNA change (hg38) g.40627100G>A
Published as LTBP4(NM_001042544.1):c.4311G>A (p.(Met1437Ile))
ISCN -
DB-ID LTBP4_000032
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) 0.00044 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.4111G>A - r.(?) p.(Gly1371Arg)
LTBP4 NM_003573.2 ?/. - c.4201G>A - r.(?) p.(Gly1401Arg)


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