Variant #0000864814 (NC_000016.9:g.46723619T>C, VPS35(NM_018206.4):c.-574A>G)
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46723619T>C |
DNA change (hg38) |
- |
Published as |
ORC6(NM_014321.3):c.2T>C (p.M1?, p.(Met1?)), ORC6(NM_014321.4):c.2T>C (p.M1?) |
ISCN |
- |
DB-ID |
ORC6_000003 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) |
0.00029 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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