All variants in the SLC29A3 gene

Information The variants shown are described using the NM_018344.5 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.946T>G r.(?) p.(Phe316Val) - likely benign g.73121883T>G g.71362126T>G SLC29A3(NM_001363518.1):c.712T>G (p.F238V), SLC29A3(NM_018344.5):c.946T>G (p.F316V) - SLC29A3_000037 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
?/. - c.946T>G r.(?) p.(Phe316Val) - VUS g.73121883T>G - SLC29A3(NM_001363518.1):c.712T>G (p.F238V), SLC29A3(NM_018344.5):c.946T>G (p.F316V) - SLC29A3_000037 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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