Variant #0000890063 (NC_000011.9:g.65306874C>T, NM_001130144.2:c.3685G>A (LTBP3))

Chromosome 11
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.65306874C>T
DNA change (hg38) -
Published as LTBP3(NM_001130144.2):c.3685G>A (p.V1229M)
ISCN -
DB-ID SCYL1_000010
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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LTBP3 NM_001130144.2 -?/. - c.3685G>A r.(?) p.(Val1229Met)
SCYL1 NM_020680.3 -?/. - c.*837C>T r.(=) p.(=)


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