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. 2010 May-Aug;16(2):67–71. doi: 10.4103/0971-6866.69348

Table 1.

Mutations/SNPs observed in both HCM and DCM

Exon Common variations
Control (n) Patient (n) NCBI accession no. in DCM
HCM DCM
7 Ala199Ala nt (7647) heterozygous Ala199Ala nt (7647) homozygous One patient each in both HCM and DCM EF630363
12 Gly354Gly (9600) heterozygous Gly354Gly(9600) homozygous 1 Six in HCM and two in DCM EF630364
Lys365Lys(9633) heterozygous Lys365Lys(9633) homozygous One in HCM and three in DCM EF630365
19 IVS19 + 92A/G homozygous IVS19 + 82A/G homozygous One each in HCM and DCM EU091312
20 IVS19 − 56A/G homozygous IVS19 − 56A/G homozygous One in HCM and two in DCM EU091314