Variant #0000966491 (NC_000011.9:g.65308047T>G, NM_001130144.2:c.3016A>C (LTBP3))

Chromosome 11
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.65308047T>G
DNA change (hg38) -
Published as LTBP3(NM_001130144.3):c.3016A>C (p.K1006Q)
ISCN -
DB-ID SCYL1_000042
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 ?/. - c.3016A>C r.(?) p.(Lys1006Gln)
SCYL1 NM_020680.3 ?/. - c.*2010T>G r.(=) p.(=)


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