Variant #0000296984 (NC_000004.11:g.111539694C>T, NM_153426.2:c.541G>A (PITX2))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.111539694C>T |
DNA change (hg38) |
g.110618538C>T |
Published as |
PITX2(NM_000325.5):c.562G>A (p.(Ala188Thr)), PITX2(NM_001204397.1):c.541G>A (p.A181T), PITX2(NM_001204397.2):c.541G>A (p.A181T) |
ISCN |
- |
DB-ID |
PITX2_000034 See all 3 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) |
0.00304 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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