Variant #0000567328 (NC_000019.9:g.39971519C>G, SUPT5H(NM_003169.3):c.*4480C>G)
Chromosome |
19 |
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.39971519C>G |
DNA change (hg38) |
g.39480879C>G |
Published as |
TIMM50(NM_001001563.1):c.335C>G (p.(Ser112Trp)) |
ISCN |
- |
DB-ID |
SUPT5H_000016 |
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) |
0.0031 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
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