Variant #0000560631 (NC_000017.10:g.18872390_18872393del, NM_152351.4:c.479_482del (SLC5A10))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18872390_18872393del |
DNA change (hg38) |
g.18969077_18969080del |
Published as |
SLC5A10(NM_152351.4):c.476_479del (p.(Phe160CysfsTer32)) |
ISCN |
- |
DB-ID |
FAM83G_000002 |
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) |
Retrieve |
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 |
2020-07-13 10:51:28 +02:00 (CEST) |

Variant on transcripts
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