Unique variants in the HSPA9 gene

Information The variants shown are described using the NM_004134.6 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Reported     

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     
./. 1 - c.-7806278_*14063202dup - - - pathogenic g.123828524_145717285dup - - - SIL1_000024 mosaicism, copy number 3 in 0.38 cells PubMed: DDDS 2015, Journal: DDDS 2015 - - Somatic - - - - - Johan den Dunnen
?/. 1 - c.26C>T r.(?) p.(Ala9Val) - VUS g.137910982G>A g.138575293G>A HSPA9(NM_004134.7):c.26C>T (p.A9V) - HSPA9_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
./. 1 - c.243C>T r.(=) p.(=) - pathogenic g.137906816G>A g.138571127G>A - - HSPA9_000001 association variant/phenotype uncertain PubMed: DDDS 2015, Journal: DDDS 2015 - - Germline - - - - - Johan den Dunnen
-?/. 1 - c.1515+7del r.(=) p.(=) - likely benign g.137894236del g.138558547del HSPA9(NM_004134.7):c.1515+7delT - HSPA9_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. 1 - c.1684G>A r.(?) p.(Val562Ile) - VUS g.137893135C>T g.138557446C>T HSPA9(NM_004134.7):c.1684G>A (p.V562I) - HSPA9_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
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