Variant #0000250704 (NC_000001.10:g.165712570del, NC_000001.10(NM_019026.4):c.477-8del (TMCO1))
Chromosome |
1 |
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.165712570del |
DNA change (hg38) |
g.165743333del |
Published as |
TMCO1(NM_001256165.1):c.288-8delT, TMCO1(NM_019026.6):c.324-8del |
ISCN |
- |
DB-ID |
TMCO1_000007 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) |
Retrieve |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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