All transcript variants in gene ATF6B

Information The variants shown are described using the NM_001136153.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.1784G>A VUS r.(?) p.(Arg595Gln) g.32084485C>T - ATF6B(NM_004381.4):c.1793G>A (p.R598Q) - ATF6B_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
-?/. - c.1793A>T likely benign r.(?) p.(His598Leu) g.32084337T>A - ATF6B(NM_001136153.1):c.1793A>T (p.(His598Leu), p.(His601Leu)) - ATF6B_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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