Variant #0000308477 (NC_000002.11:g.27423346_27423347del, NM_021095.2:c.1865_1866del (SLC5A6))
Chromosome |
2 |
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.27423346_27423347del |
DNA change (hg38) |
g.27200478_27200479del |
Published as |
SLC5A6(NM_021095.3):c.1865_1866delAG (p.Q622Rfs*51), SLC5A6(NM_021095.4):c.1865_1866del (p.(Gln622Argfs*51)), SLC5A6(NM_021095.4):c.1865_1866delAG ... |
ISCN |
- |
DB-ID |
SLC5A6_000001 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) |
4.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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