Variant #0000821072 (NC_000007.13:g.6026709G>A)

Individual ID 00390082
Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (!)
DNA change (genomic) (Relative to hg19 / GRCh37) g.6026709G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PMS2_000470 See all 5 reported entries
Variant remarks ACMG: PVS1, PS4_MOD, PM3, PM2_SUP
Reference PMID: 21618646, 22608206, 25856668, 31857677, 32906206, 20205264, 22608206
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2021-11-10 08:27:44 +01:00 (CET)
Date last edited 2021-11-10 09:13:58 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000391323 DNA SEQ-NG-I Blood WES PMS2 1 Andreas Laner


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