Variant #0000278824 (NC_000010.10:g.88439895C>T, LDB3(NM_007078.2):c.302C>T)

Chromosome 10
Allele Unknown
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.88439895C>T
DNA change (hg38) g.86680138C>T
Published as LDB3(NM_001080114.1):c.302C>T (p.(Pro101Leu)), LDB3(NM_001171610.2):c.302C>T (p.P101L), LDB3(NM_007078.2):c.302C>T (p.P101L)
ISCN -
DB-ID LDB3_000121 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0025 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDB3 NM_001080114.1 -/. - c.302C>T r.(?) p.(Pro101Leu)
LDB3 NM_007078.2 -/. - c.302C>T r.(?) p.(Pro101Leu)