Variant #0000608187 (NC_000003.11:g.101039234G>T, IMPG2(NM_016247.3):c.-18C>A)

Chromosome 3
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.101039234G>T
DNA change (hg38) g.101320390G>T
Published as IMPG2(NM_016247.3):c.-18C>A
ISCN -
DB-ID IMPG2_000087
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) 0.00025 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     
IMPG2 NM_016247.3 -?/. - c.-18C>A r.(?) p.(=)
SENP7 NM_020654.3 -?/. - c.*5553C>A r.(=) p.(=)