Variant #0000991658 (NC_000002.11:g.149247598A>G, NM_181742.3:c.-468599T>C (ORC4))
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.149247598A>G |
DNA change (hg38) |
g.148490029A>G |
Published as |
MBD5(NM_018328.4):c.3698A>G (p.(Asn1233Ser)) |
ISCN |
- |
DB-ID |
MBD5_000111 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-08-28 13:07:21 +02:00 (CEST) |
Date last edited |
2024-09-06 10:57:40 +02:00 (CEST) |

Variant on transcripts
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