Full data view for gene ARSB

Information The variants shown are described using the NM_000046.3 transcript reference sequence.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - ? - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - autism, BMD/DMD - PubMed: Bell 2011 - - - - - - 0 - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - 0 - - 1 Global Variome, with Curator vacancy
?/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - VUS g.78135241C>T g.78839418C>T - - ARSB_000001 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Global Variome, with Curator vacancy
-/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - benign g.78135241C>T g.78839418C>T ARSB(NM_000046.4):c.1151G>A (p.S384N), ARSB(NM_000046.5):c.1151G>A (p.S384N) - ARSB_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - benign g.78135241C>T g.78839418C>T ARSB(NM_000046.4):c.1151G>A (p.S384N), ARSB(NM_000046.5):c.1151G>A (p.S384N) - ARSB_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - benign g.78135241C>T g.78839418C>T ARSB 5:78170997 (hg18) het CM003999 9.6% - ARSB_000001 non-causative, heterozygous PubMed: Bell 2011 - - Germline ? - - 0 - DNA, RNA SEQ-NG blood - retinal disease NA01210 PubMed: Bell 2011 - ? - - - - 0 - - 1 LOVD
-/. - c.1151G>A r.(?) p.(Ser384Asn) Unknown - benign g.78135241C>T g.78839418C>T ARSB 5:78170997 (hg18) het CM003999 9.6% - ARSB_000001 non-causative, heterozygous PubMed: Bell 2011 - - Germline ? - - 0 - DNA, RNA SEQ-NG blood - retinal disease NA03575 PubMed: Bell 2011 - ? - - - - 0 - - 1 LOVD
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