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. 2021 Apr 9;16:166. doi: 10.1186/s13023-021-01789-2

Table 2.

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

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

gnomAD, Genome Aggregation Database