Variant #0000975193 (NC_000002.11:g.27423346_27423347del, NM_021095.2:c.1865_1866del (SLC5A6))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27423346_27423347del
DNA change (hg38) -
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC5A6 NM_021095.2 +?/. - c.1865_1866del r.(?) p.(Gln622ArgfsTer51)


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