Variant #0000515056 (NC_000002.11:g.233194516T>C, NC_000002.11(NM_152383.4):c.1740-7T>C (DIS3L2))
Chromosome |
2 |
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.233194516T>C |
DNA change (hg38) |
g.232329806T>C |
Published as |
DIS3L2(NM_152383.4):c.1740-7T>C (p.(=)), DIS3L2(NM_152383.5):c.1740-7T>C |
ISCN |
- |
DB-ID |
DIS3L2_000024 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) |
0.0018 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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