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.2060A>G benign r.(?) p.(Asp687Gly) g.79240063A>G - FRAS1:c.2060A>G (D687G) - FRAS1_000072 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.2060A>G benign r.(?) p.(Asp687Gly) g.79240063A>G - FRAS1:c.2060A>G (D687G) - FRAS1_000072 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
-/. - c.2060A>G benign r.(?) p.(Asp687Gly) g.79240063A>G - FRAS1:NM_025074.6:c.2060A>G (Asp687Gly) - FRAS1_000072 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
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