Variant #0000861934 (NC_000010.10:g.64416150T>C, NM_014951.2:c.*256602T>C (ZNF365))
Chromosome |
10 |
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.64416150T>C |
DNA change (hg38) |
- |
Published as |
ZNF365(NM_199451.3):c.1130-6T>C |
ISCN |
- |
DB-ID |
ZNF365_000005 |
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) |
0.00108 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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