Variant #0000606343 (NC_000002.11:g.170112698G>C, NM_004525.2:c.2688C>G (LRP2))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.170112698G>C |
DNA change (hg38) |
g.169256188G>C |
Published as |
LRP2(NM_004525.2):c.2688C>G (p.(His896Gln)), LRP2(NM_004525.3):c.2688C>G (p.H896Q) |
ISCN |
- |
DB-ID |
LRP2_000089 See all 3 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 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
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