Variant #0000543439 (NC_000011.9:g.20676253T>C, SLC6A5(NM_004211.3):c.2239-6T>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20676253T>C
DNA change (hg38) g.20654707T>C
Published as SLC6A5(NM_004211.5):c.2239-6T>C
ISCN -
DB-ID SLC6A5_000032
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) 0.15389 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A5 NM_004211.3 -/. - c.2239-6T>C r.(=) p.(=)