Variant #0000567321 (NC_000019.9:g.39961167T>C, SUPT5H(NM_003169.3):c.1677+4T>C)
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.39961167T>C |
DNA change (hg38) |
g.39470527T>C |
Published as |
SUPT5H(NM_001111020.2):c.1677+4T>C (p.?) |
ISCN |
- |
DB-ID |
SUPT5H_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) |
0.00161 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 |
2020-07-15 18:07:06 +02:00 (CEST) |

Variant on transcripts
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