Variant #0000649988 (NC_000019.9:g.41128415G>A, LTBP4(NM_003573.2):c.3416G>A)

Individual ID 00292131
Chromosome 19
Allele Parent #1
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.41128415G>A
DNA change (hg38) g.40622510G>A
Published as -
ISCN -
DB-ID LTBP4_000026 See all 3 reported entries
Variant remarks 233 heterozygous; Clinindb (India)
Variant Error [EMISMATCH/EREF]: This transcript variant does not match the reference sequence. Please fix this entry and then remove this message.
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs35079932
Origin Germline
Segregation -
Frequency 233/2794 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.03914 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP4 NM_003573.2 -/. - c.3416G>A - p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000293299 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq