Variant #0000311766 (NC_000018.9:g.53303101C>G, TCF4(NM_001083962.1):c.-47853G>C)
Chromosome |
18 |
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.53303101C>G |
DNA change (hg38) |
g.55635870= |
Published as |
TCF4(NM_001243226.2):c.28G>C (p.A10P) |
ISCN |
- |
DB-ID |
TCF4_000166 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.99958 View details |
Owner |
VKGL-NL_Groningen |

Variant on transcripts
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