Variant #0000658575 (NC_000019.9:g.41133759G>C, NM_001042545.1:c.4516G>C (LTBP4))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41133759G>C
DNA change (hg38) g.40627854G>C
Published as LTBP4(NM_001042544.1):c.4716G>C (p.(Val1573Leu))
ISCN -
DB-ID LTBP4_000055
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) 2.0E-5 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 2020-03-23 16:13:27 +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.4516G>C - r.(?) p.(Val1506Leu)
LTBP4 NM_003573.2 -?/. - c.4606G>C - r.(?) p.(Val1536Leu)


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