Variant #0000529862 (NC_000006.11:g.76731854G>A, NM_001563.2:c.645C>T (IMPG1))

Chromosome 6
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.76731854G>A
DNA change (hg38) g.76022137G>A
Published as IMPG1(NM_001563.3):c.645C>T (p.N215=), IMPG1(NM_001563.4):c.645C>T (p.N215=)
ISCN -
DB-ID IMPG1_000029 See all 2 reported entries
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) 0.00468 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IMPG1 NM_001563.2 -/. - c.645C>T r.(?) p.(Asn215=)


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