Variant #0000984734 (NC_000023.10:g.50350728_50350729insCC, NM_020717.3:c.3413_3414insGG (SHROOM4))
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.50350728_50350729insCC |
DNA change (hg38) |
- |
Published as |
SHROOM4(NM_020717.3):c.3413_3414insGG (p.E1140Kfs*42), SHROOM4(NM_020717.4):c.3413_3414insGG (p.(Glu1140LysfsTer42)) |
ISCN |
- |
DB-ID |
SHROOM4_000081 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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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