Variant #0000255263 (NC_000010.10:g.112769148A>G, NC_000010.10(NM_007373.3):c.1422+5A>G (SHOC2))
Chromosome |
10 |
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.112769148A>G |
DNA change (hg38) |
g.111009390A>G |
Published as |
SHOC2(NM_007373.3):c.1422+5A>G |
ISCN |
- |
DB-ID |
SHOC2_000010 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-29 11:10:00 +02:00 (CEST) |

Variant on transcripts
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