Variant #0000815712 (NC_000008.10:g.42693320T>C, NM_018105.2:c.427A>G (THAP1))
Chromosome |
8 |
Allele |
Parent #1 |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42693320T>C |
DNA change (hg38) |
g.42838177T>C |
Published as |
- |
ISCN |
- |
DB-ID |
THAP1_000023 See all 2 reported entries |
Variant remarks |
variant introduced in induced pluripotent stem cell, characterisation incl. transcript profiling |
Reference |
Journal: Domingo 2021 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2021-10-21 13:59:46 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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