Variant #0000655992 (NC_000008.10:g.12956899_12956919dup, NM_182643.2:c.2927_2947dup (DLC1))
Chromosome |
8 |
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.12956899_12956919dup |
DNA change (hg38) |
g.13099390_13099410dup |
Published as |
DLC1(NM_182643.3):c.2927_2947dupAGCCCTCCGAGATCCCGGAAA (p.E982_R983ins7) |
ISCN |
- |
DB-ID |
DLC1_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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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