Variant #0000722664 (NC_000010.10:g.111860519T>G, ADD3(NM_019903.3):c.108T>G)

Chromosome 10
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.111860519T>G
DNA change (hg38) -
Published as ADD3(NM_016824.4):c.108T>G (p.I36M)
ISCN -
DB-ID ADD3_000002
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license No license selected
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADD3 NM_019903.3 -?/. - c.108T>G r.(?) p.(Ile36Met)