Variant #0000885017 (NC_000002.11:g.232995439T>G, NC_000002.11(NM_152383.4):c.702+10T>G (DIS3L2))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.232995439T>G |
DNA change (hg38) |
- |
Published as |
DIS3L2(NM_001257282.1):c.712T>G (p.Y238D, p.(Tyr238Asp)), DIS3L2(NM_152383.4):c.702+10T>G, DIS3L2(NM_152383.5):c.702+10T>G |
ISCN |
- |
DB-ID |
DIS3L2_000013 See all 4 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) |
0.00424 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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