All variants in the NR0B1 gene

Information The variants shown are described using the NM_000475.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

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     
-?/. - c.600C>G r.(?) p.(Cys200Trp) - likely benign g.30326881G>C g.30308764G>C NR0B1(NM_000475.4):c.600C>G (p.C200W), NR0B1(NM_000475.5):c.600C>G (p.C200W) - NR0B1_000130 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.600C>G r.(?) p.(Cys200Trp) - likely benign g.30326881G>C - NR0B1(NM_000475.4):c.600C>G (p.C200W), NR0B1(NM_000475.5):c.600C>G (p.C200W) - NR0B1_000130 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Utrecht
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