Variant #0000947838 (NC_000002.11:g.3691324C>T, NM_024027.4:c.432C>T (COLEC11))
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.3691324C>T |
DNA change (hg38) |
- |
Published as |
COLEC11(NM_001255982.1):c.360C>T (p.(Ala120=)), COLEC11(NM_199235.2):c.423C>T (p.A141=), COLEC11(NM_199235.3):c.423C>T (p.A141=) |
ISCN |
- |
DB-ID |
COLEC11_000012 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) |
0.00371 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2023-11-27 17:35:39 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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