Variant #0000327486 (NC_000002.11:g.170113670G>C, NM_004525.2:c.2603C>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.170113670G>C |
DNA change (hg38) |
g.169257160G>C |
Published as |
LRP2(NM_004525.2):c.2603C>G (p.(Thr868Ser)), LRP2(NM_004525.3):c.2603C>G (p.T868S) |
ISCN |
- |
DB-ID |
LRP2_000091 See all 2 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) |
0.00095 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2019-12-04 14:54:23 +01:00 (CET) |

Variant on transcripts
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