single nucleotide variant | NM_000159.4(GCDH):c.268G>A (p.Glu90Lys) | GCDH | Likely pathogenic | 19 | 13002785 | 13002785 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA305500200 |
single nucleotide variant | NM_000159.4(GCDH):c.737C>T (p.Ser246Leu) | GCDH | Likely pathogenic | 19 | 13007120 | 13007120 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA9234477 |
single nucleotide variant | NM_000159.4(GCDH):c.956+5G>A | GCDH | Likely pathogenic | 19 | 13007832 | 13007832 | G | A | criteria provided, single submitter | ClinGen:CA645369741 |
single nucleotide variant | NM_000159.4(GCDH):c.1169G>C (p.Gly390Ala) | GCDH | Likely pathogenic | 19 | 13008603 | 13008603 | G | C | criteria provided, single submitter | ClinGen:CA16041974 |
Deletion | NM_000159.4(GCDH):c.873del (p.Asn291fs) | GCDH | Likely pathogenic | 19 | 13007744 | 13007744 | AC | A | criteria provided, single submitter | ClinGen:CA16041973 |
single nucleotide variant | NM_000159.4(GCDH):c.853-2A>G | GCDH | Likely pathogenic | 19 | 13007722 | 13007722 | A | G | criteria provided, single submitter | ClinGen:CA16041972 |
Deletion | NM_000159.4(GCDH):c.665_668del (p.Leu221_Phe222insTer) | GCDH | Likely pathogenic | 19 | 13007045 | 13007048 | CTGTT | C | criteria provided, single submitter | ClinGen:CA16041970 |
Deletion | NM_000159.4(GCDH):c.505+1_505+8del | GCDH | Likely pathogenic | 19 | 13004465 | 13004472 | CTGGGTGAG | C | criteria provided, single submitter | ClinGen:CA16041968 |
single nucleotide variant | NM_000159.4(GCDH):c.339T>G (p.Tyr113Ter) | GCDH | Likely pathogenic | 19 | 13004301 | 13004301 | T | G | criteria provided, single submitter | ClinGen:CA16041967 |
Deletion | NM_000159.4(GCDH):c.80_81del (p.Ala27fs) | GCDH | Likely pathogenic | 19 | 13002197 | 13002198 | GGC | G | criteria provided, single submitter | ClinGen:CA16041962 |