Variant #0000665605 (NC_000001.10:g.[NC_000017.10:(70900001_qter)]delins(185800001_198700000)_qter)

Individual ID 00080105
Chromosome 1
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.[NC_000017.10:(70900001_qter)]delins(185800001_198700000)_qter
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr1_013716
Variant remarks -
Reference for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin DUPLICATE record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Zeynep Tümer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-05-10 14:42:09 +02:00 (CEST)
Date last edited 2022-11-28 12:22:27 +01:00 (CET)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000080197 DNA microscope - - - 4 Zeynep Tümer


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