Variant #0000290934 (NC_000010.10:g.88428504G>C, LDB3(NM_007078.2):c.56G>C)

Chromosome 10
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.88428504G>C
DNA change (hg38) g.86668747G>C
Published as LDB3(NM_007078.2):c.56G>C (p.G19A)
ISCN -
DB-ID LDB3_000107
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LDB3 NM_001080114.1 ?/. - c.56G>C r.(?) p.(Gly19Ala)
LDB3 NM_007078.2 ?/. - c.56G>C r.(?) p.(Gly19Ala)
OPN4 NM_033282.3 ?/. - c.*2996G>C r.(=) p.(=)