Variant:
rs12721608 at chr3:119530419 in NR1I2 (VIP)

Alleles (on + chromosomal strand)
G > A
Amino Acid Translation
Arg122Gln
Alternate Names:
4321G>A, NR1I2: PXR*4, R122Q, c.365G>A, c.482G>A, g.26025565G>A, g.36089G>A, p.Arg122Gln, p.Arg161Gln

VIP Variant in NR1I2

Zhang, et al, [Article:11668216], in vitro studies identified 38 SNPs in NR1I2 several (but not all) were correlated with increased fold-induction of CYP3A4, and others with lower levels of ABCB1 induction. One variant rs12721608 (R122Q) had significantly decreased affinity for the DNA binding sequence. Zhang, et al, [Article:11668216] found that the one person heterozygous for rs12721608 (R122Q) had normal cyp3a4 metabolism.

See NR1I2 VIP summary for more information.

Cross-References

UCSC Golden Path:
chr3:119530419
dbSNP:
rs12721608

Platform Availability

  • Illumina

Common Searches

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