Variant #0000658995 (NC_000022.10:g.51136164_51136173del, NC_000022.10(NM_033517.1):c.1459+21_1459+30del (SHANK3))
Chromosome |
22 |
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.51136164_51136173del |
DNA change (hg38) |
g.50697736_50697745del |
Published as |
SHANK3(NM_001372044.2):c.1684+21_1684+30del (p.?), SHANK3(NM_001372044.2):c.1723+5_1723+14delGGGGCGCGGG |
ISCN |
- |
DB-ID |
SHANK3_000045 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_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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