Variant #0000311796 (NC_000007.13:g.100225847C>T, NM_003227.3:c.1473G>A (TFR2))
Chromosome |
7 |
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.100225847C>T |
DNA change (hg38) |
g.100628224C>T |
Published as |
TFR2(NM_003227.3):c.1473G>A (p.E491=), TFR2(NM_003227.4):c.1473G>A (p.(Glu491=), p.E491=) |
ISCN |
- |
DB-ID |
TFR2_000040 See all 8 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) |
0.00316 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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