Variant #0000299635 (NC_000011.9:g.121437819C>G, NM_003105.5:c.3220= (SORL1))
Chromosome |
11 |
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.121437819C>G |
DNA change (hg38) |
g.121567110C>G |
Published as |
SORL1(NM_003105.5):c.3220C>G (p.Q1074E) |
ISCN |
- |
DB-ID |
SORL1_000081 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) |
0.99611 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-01 16:13:22 +02:00 (CEST) |

Variant on transcripts
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