Variant #0000728123 (NC_000022.10:g.34046495C>T, LARGE(NM_004737.4):c.266G>A)
Chromosome |
22 |
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.34046495C>T |
DNA change (hg38) |
- |
Published as |
LARGE(NM_004737.4):c.266G>A (p.(Arg89Gln)), LARGE1(NM_004737.5):c.266G>A (p.R89Q) |
ISCN |
- |
DB-ID |
LARGE_000072 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 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |

Variant on transcripts
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