Full data view for gene GCDH

Variant classification: please note that where there are several records of the same variant, classification of that variant
may differ between records depending on the reporting publication or the submitter's opinion. For the curator’s opinion on
the classification, please view the SUMMARY record or the concluded functional effect (value in column Effect after the /).
Information The variants shown are described using the NM_000159.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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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     
+/+ 11 c.1168G>C r.1168g>c p.Gly390Arg Maternal (confirmed) - pathogenic (recessive) g.13008602G>C g.12897788G>C GGG>CGG (G390R) - GCDH_000008 fibroblast GCD activity undetectable PubMed: Anikster 1996 - - Germline - 1 - - - DNA, RNA RT-PCR, SEQ - - GA1 08900228-Fam8 II.1/ Table 1, Pat 8 PubMed: Mandel 1991, PubMed: Anikster 1996 This individual was first described by Mandel 1991. The mutation was identified by Anikster (a paternal muation could not be found); For pedigree see full text; Gradual improvement of motor performance after begin of dietary treatment and carnitine supplementation M yes Israel Arab muslim (family lives in a village in lower Galilee) - - - - 1 Katrin Hinderhofer
+/+ 11 c.1168G>C r.(?) p.(Gly390Arg) Unknown - pathogenic (recessive) g.13008602G>C g.12897788G>C GGG>CGG (G390R) - GCDH_000008 unaffected carrier PubMed: Anikster 1996 - - Germline/De novo (untested) - 1 - - - DNA SEQ - - - - PubMed: Anikster 1996 2nd chromosome is normal / 2-generation family8, unaffected carrier mother F yes Israel moslem, Arab - - - - 1 Katrin Hinderhofer
+/+ 11 c.1168G>C r.(?) p.(Gly390Arg) Both (homozygous) - pathogenic (recessive) g.13008602G>C g.12897788G>C - - GCDH_000008 - PubMed: Korman 2007 - - Germline - - - - - DNA SEQ blood - GA1 17188916-Pat2 PubMed: Korman 2007 - M ? Israel Palestinian Arab - - - - 1 Isabelle Rinke
+/+ 11 c.1168G>C r.(?) p.(Gly390Arg) Unknown - pathogenic (recessive) g.13008602G>C g.12897788G>C - - GCDH_000008 - PubMed: Boneh 2008 - - Germline/De novo (untested) - - - - - ? ? - - GA1 18411069-Patient 4 PubMed: Boneh 2008 Diagnosed by newborn screening; Poor compliance with treatment and clinical follow-up M ? Australia - - - - - 1 Isabelle Rinke
+/+ 11 c.1168G>C r.1168g>c p.Gly390Arg Unknown ACMG pathogenic g.13008602G>C g.12897788G>C - - GCDH_000008 ACMG/ACGS: PM5, PS4_Moderate, PM3_Supporting, PP4_Moderate, PP3_Strong, PM2_Supporting (December 2023) - - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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