Variant #0000718387 (NC_000002.11:g.204735430_204735431del, CTLA4(NM_005214.4):c.231_232del)
Chromosome |
2 |
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.204735430_204735431del |
DNA change (hg38) |
- |
Published as |
CTLA4(NM_005214.5):c.231_232delTG (p.D78Qfs*5) |
ISCN |
- |
DB-ID |
CTLA4_000009 |
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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |

Variant on transcripts
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