All variants in the SGCD gene

Information The variants shown are described using the NM_000337.5 transcript reference sequence.

27 entries on 1 page. Showing entries 1 - 27.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. 09 c.717G>? - p.Ala239Ala Substitution - GenBank SGCD_00033 - - - Qi Ming
./. 02 c.? - - Substitution - GenBank SGCD_00024 - Intron 1 (c.130G > A) - Qi Ming
./. 03 c. 84T > C - p.Tyr28Tyr Substitution - GenBank SGCD_00023 - - - Qi Ming
./. 03 c.84T>C - p.Tyr28Tyr Substitution - GenBank SGCD_00019 - Tyr28Tyr (TAT to TAC) - Qi Ming
./. 03 c.84T>C - p.Tyr28Tyr Substitution - GenBank SGCD_00019 C=0.490/590 - - Qi Ming
./. 03 c.89G>A - p.Trp30X Substitution - GenBank SGCD_00004 - p - Qi Ming
./. 04 c.212G>C - p.Arg71Thr Substitution - GenBank SGCD_00018 - Arg71Thr mutation - Qi Ming
./. 04 c.213G>A - p.Arg71Arg Substitution - GenBank SGCD_00026 - - - Qi Ming
./. 04 c.267C>T - p.Leu89Leu Substitution - GenBank SGCD_00027 - - - Qi Ming
./. 04 c.277G>T - p.Glu93X Substitution - GenBank SGCD_00005 - - - Qi Ming
./. 04 c.290G>A - p.Arg97Gln Substitution - GenBank SGCD_00019 - Arg97Gln (CGA to CAA) - Qi Ming
./. 04 c.290G>A - p.Arg97Gln Substitution - GenBank SGCD_00019 - - - Qi Ming
./. 04 c.290G>A - p.Arg97Gln Substitution - GenBank SGCD_00019 0.0199 - - Qi Ming
./. 05 c.295-38T>A - - Substitution - GenBank SGCD_00021 - - - Qi Ming
./. 05 c.382+1_382+2del - - Deletion - GenBank SGCD_00022 - - - Qi Ming
./. 06 c.386C>A - p.Pro129Gln Substitution - GenBank SGCD_00028 - - - Qi Ming
./. 06 c.387A>C - p.Pro129Pro Substitution - GenBank SGCD_00029 - - - Qi Ming
./. 06 c.391G>C - p.Ala131Pro Substitution - GenBank SGCD_00025 - a single nucleotide substitution at position 391 (G for C) - Qi Ming
./. 06 c.451T>G - p.Ser151Ala Substitution - GenBank SGCD_00018 - - - Qi Ming
./. 06 c.451T>G - p.Ser151Ala Substitution - GenBank SGCD_00018 - a single nucleotide (T for G) resulting in an amino-acid change from serine to alanine at codon 151 - Qi Ming
./. 06 c.493C>T - p.Arg165X Substitution - GenBank SGCD_00003 - C?T point mutation - Qi Ming
./. 07 c.507G>A - p.Ala169Ala Substitution - GenBank SGCD_00030 - - - Qi Ming
./. 08 c.601delG - p.Val201X Deletion - GenBank SGCD_00031 - - - Qi Ming
./. 08 c.656delC - p.Thr220ProfsX6 Deletion - GenBank SGCD_00001 - - - Qi Ming
./. 09 c.710_712del - p.Lys238del Deletion - GenBank SGCD_00020 - a 3-bp deletion (either 710 - Qi Ming
./. 09 c.717G>A - p.Ala239Ala Substitution - GenBank SGCD_00032 - - - Qi Ming
./. 09 c.784G>A - p.Glu262Lys Substitution - GenBank SGCD_00002 - C>A transtransversion at position 784 of the cDNA - Qi Ming
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