All variants in the SLC6A5 gene

Information The variants shown are described using the NM_004211.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.395C>G r.(?) p.(Ala132Gly) - likely benign g.20623066C>G g.20601520C>G SLC6A5(NM_004211.5):c.395C>G (p.A132G) - SLC6A5_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
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