Variant #0000039989 (NC_000006.11:g.18139200C>G, NM_000367.2:c.488G>C (TPMT))
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18139200C>G |
DNA change (hg38) |
g.18138969C>G |
Published as |
- |
ISCN |
- |
DB-ID |
TPMT_000220 See all 3 reported entries |
Variant remarks |
expression cloning COS7-cells, reduced protein expression, no activity in 6-TG S-methylation |
Reference |
PubMed: Ujiie 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2013-01-11 21:07:51 +01:00 (CET) |
Date last edited |
2020-07-14 22:00:02 +02:00 (CEST) |

Variant on transcripts
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