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Table 3 New variants (not described previously in literature)

From: ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

Gene

Patient

Inheritance

Type

Nomenclature

Classification ACMG

ACER3

IDSPG75

AR

Missense

NP_060837.3:p.(Gly211Cys)

Pathogenic

AMPD2

IDSPG78

AR

Frameshift deletion

NP_631895.1:p.(Ala62SerfsTer40)

Pathogenic

BCKDK

IDSPG47.0

AR

Missense

NP_005872.2:p.(Arg327Trp)

Likely pathogenic

CAPN10

IDSPG47.1

AR

Splicing

NM_023083.3:c.1989 + 1G > A

Pathogenic

DLG4

IDSPG107

AD

Splicing

NM_001365.4:c.1721-1G > A

Pathogenic

ERBB4

IDSPG38

AD

Non-canonical splicing

NM_005235.2:c.2487 + 8_2487 + 11dell

VUS

FA2H

IDSPG10

AR

Missense

NP_077282.3:p.(Lys262Thr)

Likely pathogenic

GFAP

IDSPG4

AD

Missense

NP_001124491.1:p.(Gly18Val)

Pathogenic

IFIH1

IDSPG3

AD

Missense

NP_071451.2:p.(Leu320Phe)

VUS

KCNA1

IDLNF52

AR

Missense

NP_000208.2:p.(Val368Leu))

Pathogenic

KIDINS220

IDSPG118

AD

Splicing

NM_020738.3:c.4054-1G > C

Likely pathogenic

KIF5A

IDSPG17

AD

Missense

NP_004975.2:p.(Gly246Val)

Pathogenic

KMT2B

IDSPG114

AD

Missense

NP_055542.1:p.(Ala1727Ser)

Likely pathogenic

LAMA1

IDSPG56

AR

Frameshift insertion

NP_005550.2:p.(Gly2899GlufsTer18)

Pathogenic

LAMA1

IDSPG56

AR

Non-canonical splicing

NM_005559.3:c.1423-12C > G

Pathogenic

LONP1

IDSPG166

AR

Splicing

NM_004793.3:c.2154 + 1G > C

Pathogenic

LONP1

IDSPG166

AR

Missense

NP_004784.2:p.(Leu306Trp)

Likely pathogenic

PCYT2

IDSPG27

AR

Missense, splicing

NP_001171846.1:p.(Lys319Asn)

Likely pathogenic

PI4KA

IDSPG16

AR

Frameshift deletion

NP_477352.3:p.(Thr2053SerfsTer4)

Pathogenic

PI4KA

IDSPG16

AR

Frameshift deletion

NP_477352.3:p.(Glu1820del)

Pathogenic

PI4KA

IDSPG149

AR

Missense

NP_477352.3:p.(Val1556Met)

Pathogenic

PI4KA

IDSPG149

AR

Missense

NP_477352.3:p.(Thr1720Ile)

Pathogenic

PNPLA6

IDSPG13

AR

Splicing

NM_006702.4:c.598-2A > C

Pathogenic

PNPLA6

IDSPG13

AR

Missense

NP_001159586.1:p.(Ser1138Cys)

Likely pathogenic

POLG

IDSPG113

AR

Non-canonical splicing

NM_002693.2:c.2266-64C > T

VUS

POLR3B

IDSPG66

AD

Missense

NP_060552.4:p.(Ala69Gly)

VUS

REEP1

IDSPG12

AD

Missense

NP_075063.1:p.(Leu59His)

Likely pathogenic

SARS1

IDSPG64

AD

Splicing

NM_006513.4:c.969 + 1_969 + 3del

Pathogenic

SHMT2

IDSPG26

AR

Missense

NP_005403.2:p.(Pro499Ala)

Likely pathogenic

SLC35B2

IDLNF68

AR

Frameshift deletion

NP_835361.1:p.Arg408SerfsTer18

Pathogenic

SPG7

IDSPG23

AR

Non frameshift deletion

NP_003110.1:p.(Val311del)

Likely pathogenic

SPG7

IDSPG30

AR

Missense

NP_003110.1:p.(Met667Ile))

Likely pathogenic

SPTBN2

IDSPG125

AD

Frameshift deletion

NP_008877.1:p.(Asp1861ThrfsTer59)

Pathogenic

SVBP

IDSPG8,IDSPG46

AR

Missense

NP_955374.1:p.(Leu49Pro)

Likely pathogenic

TAF1

IDSPG71

XL

Missense

NP_001273003.1:p.(Ala1732Ser)

VUS

UBAP1

IDSPG76

AD

Frameshift deletion

NP_057609.2:p.(Phe159Ter)

Pathogenic

  1. AD autosomal dominant, AR autosomal recessive, SNV single-nucleotide variant, VUS variant of unknown significance
  2. List with the 36 SNV/INDEL new variants identified in our cohort, classification according to ACMG criteria