Variant #0000924252 (NC_000005.9:g.138386706G>A, NM_001037633.1:c.274C>T (SIL1))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.138386706G>A |
DNA change (hg38) |
- |
Published as |
SIL1(NM_001037633.1):c.274C>T (p.R92W), SIL1(NM_022464.5):c.274C>T (p.R92W) |
ISCN |
- |
DB-ID |
SIL1_000018 See all 4 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) |
0.00502 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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