Variant #0000518000 (NC_000003.11:g.133465283A>G, TF(NM_001063.3):c.-2A>G)
Chromosome |
3 |
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.133465283A>G |
DNA change (hg38) |
g.133746439A>G |
Published as |
TF(NM_001063.3):c.-2A>G |
ISCN |
- |
DB-ID |
TF_000005 See all 2 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) |
0.59966 View details |
Owner |
VKGL-NL_Nijmegen |

Variant on transcripts
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