Variant #0000655709 (NC_000007.13:g.110764681A>C, NC_000007.13(NM_032549.3):c.240-161060T>G (IMMP2L))
Chromosome |
7 |
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.110764681A>C |
DNA change (hg38) |
g.111124625A>C |
Published as |
LRRN3(NM_001099660.1):c.1853A>C (p.Q618P) |
ISCN |
- |
DB-ID |
IMMP2L_000009 |
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) |
0.00021 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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