Variant #0000249863 (NC_000023.10:g.132888223del, NC_000023.10(NM_004484.3):c.338-5del (GPC3))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.132888223del |
DNA change (hg38) |
g.133754196del |
Published as |
GPC3(NM_001164617.1):c.338-5del (p.?), GPC3(NM_001164617.1):c.338-5delT, GPC3(NM_001164617.2):c.338-5delT, GPC3(NM_004484.4):c.338-5delT |
ISCN |
- |
DB-ID |
GPC3_000073 See all 4 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) |
Retrieve |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
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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