Table 2: Genetic variants detected in NR1C3.

SNP no.Position in DNA( a)Exon/ intron no.Exon positionIntron/ exonBase exchangePosition in RNA(b)AA exchange(c)SNP database

1123329791IntronG>TNANot found
2123330681ExoninsC68frame shiftNot found
31233307015-primeC>T705-primeNot found
412333125112333001–12333173ExonC>G12512 P [Pro]>A [Ala]rs1801282
5123331991IntronT>GNANot found
6123332131IntronG>ANANot found
712361272212361203–12361430ExonC>T24351 S [Ser]>F [Phe]Not found
8123614222ExonA>G393101 E [Glu]>G [Gly]Not found
912363017312362821–12362990IntronA>GNANot found
10123740144IntronG>TNANot found
11123740244IntronA>TNANot found
12123740914IntronC>ANArs4135333
13123741104IntronC>TNANot found
1412374272412374113–12374251IntronA>TNArs4135334
15123743524IntronC>TNANot found
1612387616512387381–12387580IntronG>ANANot found
1712398613612398203–12398653ExonC>T1321410 S [Ser]>S [Ser]Not found
18124154737ExonG>A1438449 L [Leu]>L [Leu]Not found
1912415557712415397–12415855ExonC>T1522477 H [His]>H [His]rs3856806
20124155817ExonG>A1546485 K [Lys]>K [Lys]Not found
21124156477ExonG>A1611506 stop>stopNot found
221241566973′ endC>T3′ endNot found

no.: number; AA: amino acid; (a)DNA reference sequence NT_02257.18; (b)RNA reference sequence NM_015869.4; (c)protein reference sequence P37231 (PPARG_HUMAN) SWISSPROT database.