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Table 2 Pathogenic variants and likely pathogenic variants of East Asian and Korean in gnomAD population

From: Carrier frequency and incidence estimation of Smith–Lemli–Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis

Nucleotide change Amino acid change gnomAD allele frequency (allele count/allele number)
Korean (n = 1909) East Asain (n = 9197) African
(n = 8128)
Latino
(n = 17,296)
Ashkenazi Jewish
(n = 5040)
European (Finnish)
(n = 10,824)
European (non-Finnish)
(n = 56,885)
Other
(n = 3070)
South Asian
(n = 15,308)
c.16 C > T p.Gln6Ter 0 5.437E−05
(1/18,394)
0 0 0 0 0 0 0
c.356 A > G p.His119Arg 0 5.44E−05
(1/18,382)
0 0 0 0 7.046E−05
(8/113,532)
0 0.00026228
(8/30,502)
c.724 C > T p.Arg242Cys 0 5.437E−05
(1/18,394)
0.0001847
(3/16,244)
0 0 0 0.0001672
(19/113,650)
0.0001630
(1/6,136)
3.2663E−05
(1/30,616)
c.725G > A p.Arg242His 0 5.437E−05
(1/18,394)
0 0 0 0 3.52E−05
(4/113,650)
0 0
c.730G > A p.Gly244Arg 0 5.437E−05
(1/18,392)
0 0 0 0 8.8E−06
(1/113,638)
0 0.0001960
(6/30,616)
c.852 C > A p.Phe284Leu 0 5.446E−05
(1/18,362)
0 0 0 0 0 0 0
c.860 A > G p.Asn287Ser 0 5.444E−05
(1/18,370)
0 0 0 0 0 0 0
c.907G > A p.Gly303Arg 0.0026192
(10/3,818)
0.0005439
(10/18,386)
0.0002461
(4/16,254)
2.892E-05
(1/34,580)
0 4.634E-05
(1/21,578)
6.156E−05
(7/113,704)
0 0
c.1055G > A p.Arg352Gln 0.0002622
(1/3,814)
5.473E−05
(1/18,270)
0.0001248
(2/16,022)
0 0 0 1.786E−05
(2/111,962)
0 3.2686E−05
(1/30,594)
c.1084 C > A p.Arg362Ser 0 5.462E-05
(1/18,308)
0 0 0 0 0 0 0
c.1085G > A p.Arg362His 0 5.46E−05
(1/18,316)
0 0 0 0 4.475E−05
(5/111,722)
0 9.8026E−05
(3/30,604)
c.1139G > T p.Cys380Phe 0.001048
(4/3,816)
0.0002188
(4/18,280)
0 0 0 0 0 0 0
c.1140 C > A p.Cys380Ter 0.001048
(4/3,818)
0.0002187
(4/18,286)
0 0 0 0 0 0 0
c.1190 C > T p.Ser397Leu 0 5.541E−05
(1/18,046)
0 0 0 0 1.833E−05
(2/109,128)
0 0
c.1426T > C p.Ter476GlnextTer51 0 0.0002189
(4/18,276)
0 0 0 0 0 0 0
  1. gnomAD, Genome Aggregation Database
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