All transcript variants in gene IQSEC2

Information The variants shown are described using the NM_001111125.1 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.2278G>A likely pathogenic (dominant) r.(?) p.(Gly760Ser) g.53279480C>T - IQSEC2(NM_001111125.2):c.2278G>A (p.G760S) - IQSEC2_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
+?/. - c.2278G>A likely pathogenic (dominant) r.(?) p.(Gly760Ser) g.53279480C>T - IQSEC2(NM_001111125.2):c.2278G>A (p.G760S) - IQSEC2_000040 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Nijmegen
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