Variant #0000543936 (NC_000011.9:g.45827855_45827857del, NM_018389.4:c.503_505del (SLC35C1))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45827855_45827857del |
DNA change (hg38) |
g.45806304_45806306del |
Published as |
SLC35C1(NM_001145265.1):c.464_466del (p.(Phe155del)), SLC35C1(NM_018389.4):c.503_505delTCT (p.F168del), SLC35C1(NM_018389.5):c.503_505delTCT (p.F1...) |
ISCN |
- |
DB-ID |
SLC35C1_000005 See all 3 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|