All transcript variants in gene FRAS1

Information The variants shown are described using the NM_025074.6 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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.776T>G likely benign r.(?) p.(Leu259Arg) g.79188076T>G - FRAS1:c.776T>G (L259R) - FRAS1_000039 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
-/. - c.776T>G benign r.(?) p.(Leu259Arg) g.79188076T>G - FRAS1:c.776T>G (L259R) - FRAS1_000039 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.776T>G likely benign r.(?) p.(Leu259Arg) g.79188076T>G - FRAS1:NM_001166133.1:c.776T>G, NM_025074.6:c.776T>G - FRAS1_000039 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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