11-63671570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671570
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671570
    reference: chr 11
allele count: 14
allele frequency: 1.754166144593409e-4
allele num: 79810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1525G>A
  hgvsp: ENSP00000423974.2:p.Ala509Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1528G>A
  hgvsp: ENSP00000421075.2:p.Ala510Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1387G>A
  hgvsp: ENSP00000415494.2:p.Ala463Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1624G>A
  hgvsp: ENSP00000423452.3:p.Ala542Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1627G>A
  hgvsp: ENSP00000385751.2:p.Ala543Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1627G>A
  hgvsp: ENSP00000367040.4:p.Ala543Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-688G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1627G>A
  hgvsp: ENSP00000326632.8:p.Ala543Thr
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8488
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12335
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala543Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-63671583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671583
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 68366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-675C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1640C>T
  hgvsp: ENSP00000385751.2:p.Pro547Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1541C>T
  hgvsp: ENSP00000421075.2:p.Pro514Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-675C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-675C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1538C>T
  hgvsp: ENSP00000423974.2:p.Pro513Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1637C>T
  hgvsp: ENSP00000423452.3:p.Pro546Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1640C>T
  hgvsp: ENSP00000367040.4:p.Pro547Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1400C>T
  hgvsp: ENSP00000415494.2:p.Pro467Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1640C>T
  hgvsp: ENSP00000326632.8:p.Pro547Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-675C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-675C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-675C>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro547Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

11-63671590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671590
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671590
    reference: chr 11
allele count: 1
allele frequency: 1.578033769922677e-5
allele num: 63370
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1647G>A
  hgvsp: ENST00000402010.2:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-668G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1545G>A
  hgvsp: ENST00000509502.2:c.1545G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-668G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-668G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-668G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1644G>A
  hgvsp: ENST00000502399.3:c.1644G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1407G>A
  hgvsp: ENST00000425897.2:c.1407G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-668G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1548G>A
  hgvsp: ENST00000513765.2:c.1548G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1647G>A
  hgvsp: ENST00000315032.8:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1647G>A
  hgvsp: ENST00000377809.4:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-668G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16533
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr549Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-63671601-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671601
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671601
    reference: chr 11
allele count: 1
allele frequency: 1.866019779809666e-5
allele num: 53590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-657G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1556G>T
  hgvsp: ENSP00000423974.2:p.Cys519Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1658G>T
  hgvsp: ENSP00000326632.8:p.Cys553Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1658G>T
  hgvsp: ENSP00000385751.2:p.Cys553Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1655G>T
  hgvsp: ENSP00000423452.3:p.Cys552Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1658G>T
  hgvsp: ENSP00000367040.4:p.Cys553Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1418G>T
  hgvsp: ENSP00000415494.2:p.Cys473Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-657G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1559G>T
  hgvsp: ENSP00000421075.2:p.Cys520Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-657G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-657G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-657G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-657G>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys553Phe
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

11-63671610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671610
    reference: chr 11
allele count: 1
allele frequency: 2.239140170174653e-5
allele num: 44660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1667C>T
  hgvsp: ENSP00000326632.8:p.Pro556Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1568C>T
  hgvsp: ENSP00000421075.2:p.Pro523Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1667C>T
  hgvsp: ENSP00000367040.4:p.Pro556Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-648C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-648C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-648C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-648C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1664C>T
  hgvsp: ENSP00000423452.3:p.Pro555Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1667C>T
  hgvsp: ENSP00000385751.2:p.Pro556Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1565C>T
  hgvsp: ENSP00000423974.2:p.Pro522Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1427C>T
  hgvsp: ENSP00000415494.2:p.Pro476Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-648C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-648C>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro556Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

11-63671611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671611
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671611
    reference: chr 11
allele count: 3
allele frequency: 7.041922914417163e-5
allele num: 42602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1569G>A
  hgvsp: ENST00000513765.2:c.1569G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1668G>A
  hgvsp: ENST00000402010.2:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1665G>A
  hgvsp: ENST00000502399.3:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1668G>A
  hgvsp: ENST00000315032.8:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1668G>A
  hgvsp: ENST00000377809.4:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1566G>A
  hgvsp: ENST00000509502.2:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-647G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1428G>A
  hgvsp: ENST00000425897.2:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro556Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-63671626-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671626
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671626
    reference: chr 11
allele count: 6
allele frequency: 1.770015930143371e-4
allele num: 33898
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1676+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1436+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1574+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-632G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-632G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1673+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1577+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-632G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-632G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1676+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1676+7G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-632G>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-632G>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22921
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1676+7G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

11-63671642-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671642
    reference: chr 11
allele count: 1
allele frequency: 4.05120725976341e-5
allele num: 24684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1577+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-616T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1574+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1676+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1436+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-616T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-616T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-616T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-616T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1676+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1673+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1676+23T>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-616T>G
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

11-63671644-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671644
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671644
    reference: chr 11
allele count: 1
allele frequency: 4.127115146512587e-5
allele num: 24230
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1676+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1676+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1676+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1574+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1673+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1577+25C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-614C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1436+25C>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-63671645-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671645
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671645
    reference: chr 11
allele count: 26
allele frequency: 1.083513918986498e-3
allele num: 23996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-613A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-613A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-613A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1574+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-613A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1436+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1676+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-613A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1673+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1676+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1577+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1676+26A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-613A>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 27351
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17569
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-63671659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63671659
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63671659
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-599G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1574+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-599G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1673+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1436+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-599G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-599G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-599G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1577+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1676+40G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-599G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30856
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

11-63672209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672209
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672209
    reference: chr 11
allele count: 1
allele frequency: 8.464390309965973e-6
allele num: 118142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-49T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-49T>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum

11-63672214-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672214
    reference: chr 11
allele count: 1
allele frequency: 8.45508658008658e-6
allele num: 118272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-44T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-44T>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

11-63672224-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672224
    reference: chr 11
allele count: 2
allele frequency: 1.684664499065011e-5
allele num: 118718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-34T>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-34T>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-63672226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672226
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672226
    reference: chr 11
allele count: 1
allele frequency: 8.416233230655287e-6
allele num: 118818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-32C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-32C>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-63672227-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672227
    reference: chr 11
allele count: 5
allele frequency: 4.201821909980167e-5
allele num: 118996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-31G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-31G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

11-63672233-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672233
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672232
    reference: chr 11
allele count: 19
allele frequency: 1.585738369860956e-4
allele num: 119818
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-24delT
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-24delT
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: CT
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

11-63672248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672248
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672248
    reference: chr 11
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1578-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1575-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1515-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1677-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1677-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1512-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1677-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1413-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1413-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1515-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1674-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1512-10C>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1437-10C>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-63672267-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672267
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672267
    reference: chr 11
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1686C>G
  hgvsp: ENST00000377809.4:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1524C>G
  hgvsp: ENST00000361128.5:c.1524C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1524C>G
  hgvsp: ENST00000413835.2:c.1524C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1686C>G
  hgvsp: ENST00000315032.8:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1521C>G
  hgvsp: ENST00000350490.7:c.1521C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1446C>G
  hgvsp: ENST00000425897.2:c.1446C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1521C>G
  hgvsp: ENST00000508192.1:c.1521C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1587C>G
  hgvsp: ENST00000513765.2:c.1587C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1422C>G
  hgvsp: ENST00000408948.3:c.1422C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1686C>G
  hgvsp: ENST00000402010.2:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1584C>G
  hgvsp: ENST00000509502.2:c.1584C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1683C>G
  hgvsp: ENST00000502399.3:c.1683C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1422C>G
  hgvsp: ENST00000377810.3:c.1422C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro562Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

11-63672271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672271
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672271
    reference: chr 11
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1528C>T
  hgvsp: ENSP00000355091.5:p.Arg510Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1528C>T
  hgvsp: ENSP00000389184.2:p.Arg510Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1690C>T
  hgvsp: ENSP00000367040.4:p.Arg564Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1525C>T
  hgvsp: ENSP00000294247.9:p.Arg509Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1690C>T
  hgvsp: ENSP00000326632.8:p.Arg564Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1588C>T
  hgvsp: ENSP00000423974.2:p.Arg530Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1525C>T
  hgvsp: ENSP00000425765.1:p.Arg509Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1426C>T
  hgvsp: ENSP00000386128.3:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1450C>T
  hgvsp: ENSP00000415494.2:p.Arg484Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1687C>T
  hgvsp: ENSP00000423452.3:p.Arg563Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1591C>T
  hgvsp: ENSP00000421075.2:p.Arg531Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1426C>T
  hgvsp: ENSP00000367041.3:p.Arg476Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1690C>T
  hgvsp: ENSP00000385751.2:p.Arg564Cys
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg564Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-63672272-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672272
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672272
    reference: chr 11
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1688G>A
  hgvsp: ENSP00000423452.3:p.Arg563His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1691G>A
  hgvsp: ENSP00000367040.4:p.Arg564His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1451G>A
  hgvsp: ENSP00000415494.2:p.Arg484His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1427G>A
  hgvsp: ENSP00000386128.3:p.Arg476His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1529G>A
  hgvsp: ENSP00000355091.5:p.Arg510His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1526G>A
  hgvsp: ENSP00000294247.9:p.Arg509His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1589G>A
  hgvsp: ENSP00000423974.2:p.Arg530His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1691G>A
  hgvsp: ENSP00000326632.8:p.Arg564His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1526G>A
  hgvsp: ENSP00000425765.1:p.Arg509His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1592G>A
  hgvsp: ENSP00000421075.2:p.Arg531His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1529G>A
  hgvsp: ENSP00000389184.2:p.Arg510His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1691G>A
  hgvsp: ENSP00000385751.2:p.Arg564His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1427G>A
  hgvsp: ENSP00000367041.3:p.Arg476His
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg564His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

11-63672276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672276
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672276
    reference: chr 11
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1530C>T
  hgvsp: ENST00000508192.1:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1431C>T
  hgvsp: ENST00000377810.3:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1692C>T
  hgvsp: ENST00000502399.3:c.1692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1695C>T
  hgvsp: ENST00000377809.4:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1695C>T
  hgvsp: ENST00000315032.8:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1455C>T
  hgvsp: ENST00000425897.2:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1533C>T
  hgvsp: ENST00000361128.5:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1431C>T
  hgvsp: ENST00000408948.3:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1533C>T
  hgvsp: ENST00000413835.2:c.1533C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1593C>T
  hgvsp: ENST00000509502.2:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1596C>T
  hgvsp: ENST00000513765.2:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1530C>T
  hgvsp: ENST00000350490.7:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1695C>T
  hgvsp: ENST00000402010.2:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val565Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

11-63672294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672294
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672294
    reference: chr 11
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1713C>T
  hgvsp: ENST00000402010.2:c.1713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1611C>T
  hgvsp: ENST00000509502.2:c.1611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1449C>T
  hgvsp: ENST00000408948.3:c.1449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1548C>T
  hgvsp: ENST00000508192.1:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1713C>T
  hgvsp: ENST00000377809.4:c.1713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1551C>T
  hgvsp: ENST00000361128.5:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1710C>T
  hgvsp: ENST00000502399.3:c.1710C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1551C>T
  hgvsp: ENST00000413835.2:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1713C>T
  hgvsp: ENST00000315032.8:c.1713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1548C>T
  hgvsp: ENST00000350490.7:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1473C>T
  hgvsp: ENST00000425897.2:c.1473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1449C>T
  hgvsp: ENST00000377810.3:c.1449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1614C>T
  hgvsp: ENST00000513765.2:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser571Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

11-63672295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672295
    reference: chr 11
allele count: 2
allele frequency: 1.649729444371123e-5
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1450G>A
  hgvsp: ENSP00000386128.3:p.Ala484Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1474G>A
  hgvsp: ENSP00000415494.2:p.Ala492Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1714G>A
  hgvsp: ENSP00000367040.4:p.Ala572Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1450G>A
  hgvsp: ENSP00000367041.3:p.Ala484Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1711G>A
  hgvsp: ENSP00000423452.3:p.Ala571Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1714G>A
  hgvsp: ENSP00000385751.2:p.Ala572Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1714G>A
  hgvsp: ENSP00000326632.8:p.Ala572Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1612G>A
  hgvsp: ENSP00000423974.2:p.Ala538Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1549G>A
  hgvsp: ENSP00000294247.9:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1552G>A
  hgvsp: ENSP00000389184.2:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1549G>A
  hgvsp: ENSP00000425765.1:p.Ala517Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1552G>A
  hgvsp: ENSP00000355091.5:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1615G>A
  hgvsp: ENSP00000421075.2:p.Ala539Thr
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala572Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

11-63672295-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672295
    reference: chr 11
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1549G>T
  hgvsp: ENSP00000294247.9:p.Ala517Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1549G>T
  hgvsp: ENSP00000425765.1:p.Ala517Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1450G>T
  hgvsp: ENSP00000386128.3:p.Ala484Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1615G>T
  hgvsp: ENSP00000421075.2:p.Ala539Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1552G>T
  hgvsp: ENSP00000389184.2:p.Ala518Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1714G>T
  hgvsp: ENSP00000367040.4:p.Ala572Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1714G>T
  hgvsp: ENSP00000326632.8:p.Ala572Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1612G>T
  hgvsp: ENSP00000423974.2:p.Ala538Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1711G>T
  hgvsp: ENSP00000423452.3:p.Ala571Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1474G>T
  hgvsp: ENSP00000415494.2:p.Ala492Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1450G>T
  hgvsp: ENSP00000367041.3:p.Ala484Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1714G>T
  hgvsp: ENSP00000385751.2:p.Ala572Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1552G>T
  hgvsp: ENSP00000355091.5:p.Ala518Ser
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala572Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

11-63672304-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672304
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672304
    reference: chr 11
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1624A>G
  hgvsp: ENSP00000421075.2:p.Ile542Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1561A>G
  hgvsp: ENSP00000389184.2:p.Ile521Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1621A>G
  hgvsp: ENSP00000423974.2:p.Ile541Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1483A>G
  hgvsp: ENSP00000415494.2:p.Ile495Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1558A>G
  hgvsp: ENSP00000294247.9:p.Ile520Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1723A>G
  hgvsp: ENSP00000326632.8:p.Ile575Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1723A>G
  hgvsp: ENSP00000367040.4:p.Ile575Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1558A>G
  hgvsp: ENSP00000425765.1:p.Ile520Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1723A>G
  hgvsp: ENSP00000385751.2:p.Ile575Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1561A>G
  hgvsp: ENSP00000355091.5:p.Ile521Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1459A>G
  hgvsp: ENSP00000367041.3:p.Ile487Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1720A>G
  hgvsp: ENSP00000423452.3:p.Ile574Val
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1459A>G
  hgvsp: ENSP00000386128.3:p.Ile487Val
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile575Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

11-63672307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672307
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672307
    reference: chr 11
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1564A>G
  hgvsp: ENSP00000389184.2:p.Ser522Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1726A>G
  hgvsp: ENSP00000367040.4:p.Ser576Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1723A>G
  hgvsp: ENSP00000423452.3:p.Ser575Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1462A>G
  hgvsp: ENSP00000367041.3:p.Ser488Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1462A>G
  hgvsp: ENSP00000386128.3:p.Ser488Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1627A>G
  hgvsp: ENSP00000421075.2:p.Ser543Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1564A>G
  hgvsp: ENSP00000355091.5:p.Ser522Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1486A>G
  hgvsp: ENSP00000415494.2:p.Ser496Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1624A>G
  hgvsp: ENSP00000423974.2:p.Ser542Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1726A>G
  hgvsp: ENSP00000326632.8:p.Ser576Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1726A>G
  hgvsp: ENSP00000385751.2:p.Ser576Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1561A>G
  hgvsp: ENSP00000425765.1:p.Ser521Gly
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1561A>G
  hgvsp: ENSP00000294247.9:p.Ser521Gly
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser576Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-63672309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672309
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672309
    reference: chr 11
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1626C>T
  hgvsp: ENST00000509502.2:c.1626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1566C>T
  hgvsp: ENST00000413835.2:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1464C>T
  hgvsp: ENST00000377810.3:c.1464C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1566C>T
  hgvsp: ENST00000361128.5:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1728C>T
  hgvsp: ENST00000402010.2:c.1728C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1464C>T
  hgvsp: ENST00000408948.3:c.1464C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1728C>T
  hgvsp: ENST00000377809.4:c.1728C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1488C>T
  hgvsp: ENST00000425897.2:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1563C>T
  hgvsp: ENST00000508192.1:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1563C>T
  hgvsp: ENST00000350490.7:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1725C>T
  hgvsp: ENST00000502399.3:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1629C>T
  hgvsp: ENST00000513765.2:c.1629C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1728C>T
  hgvsp: ENST00000315032.8:c.1728C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser576Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-63672316-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672316
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672316
    reference: chr 11
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1732G>C
  hgvsp: ENSP00000423452.3:p.Gly578Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1570G>C
  hgvsp: ENSP00000425765.1:p.Gly524Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1633G>C
  hgvsp: ENSP00000423974.2:p.Gly545Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1636G>C
  hgvsp: ENSP00000421075.2:p.Gly546Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1471G>C
  hgvsp: ENSP00000367041.3:p.Gly491Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1495G>C
  hgvsp: ENSP00000415494.2:p.Gly499Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1735G>C
  hgvsp: ENSP00000385751.2:p.Gly579Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1573G>C
  hgvsp: ENSP00000389184.2:p.Gly525Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1573G>C
  hgvsp: ENSP00000355091.5:p.Gly525Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1735G>C
  hgvsp: ENSP00000326632.8:p.Gly579Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1570G>C
  hgvsp: ENSP00000294247.9:p.Gly524Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1735G>C
  hgvsp: ENSP00000367040.4:p.Gly579Arg
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1471G>C
  hgvsp: ENSP00000386128.3:p.Gly491Arg
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly579Arg
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

11-63672316-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672316
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672316
    reference: chr 11
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1573G>T
  hgvsp: ENSP00000389184.2:p.Gly525Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1633G>T
  hgvsp: ENSP00000423974.2:p.Gly545Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1732G>T
  hgvsp: ENSP00000423452.3:p.Gly578Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1573G>T
  hgvsp: ENSP00000355091.5:p.Gly525Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1471G>T
  hgvsp: ENSP00000386128.3:p.Gly491Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1471G>T
  hgvsp: ENSP00000367041.3:p.Gly491Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1570G>T
  hgvsp: ENSP00000294247.9:p.Gly524Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1570G>T
  hgvsp: ENSP00000425765.1:p.Gly524Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1735G>T
  hgvsp: ENSP00000367040.4:p.Gly579Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1636G>T
  hgvsp: ENSP00000421075.2:p.Gly546Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1735G>T
  hgvsp: ENSP00000326632.8:p.Gly579Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1735G>T
  hgvsp: ENSP00000385751.2:p.Gly579Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1495G>T
  hgvsp: ENSP00000415494.2:p.Gly499Cys
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly579Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

11-63672317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672317
    reference: chr 11
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1637G>A
  hgvsp: ENSP00000421075.2:p.Gly546Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1736G>A
  hgvsp: ENSP00000385751.2:p.Gly579Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1736G>A
  hgvsp: ENSP00000367040.4:p.Gly579Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1472G>A
  hgvsp: ENSP00000386128.3:p.Gly491Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1733G>A
  hgvsp: ENSP00000423452.3:p.Gly578Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1496G>A
  hgvsp: ENSP00000415494.2:p.Gly499Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1736G>A
  hgvsp: ENSP00000326632.8:p.Gly579Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1574G>A
  hgvsp: ENSP00000389184.2:p.Gly525Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1574G>A
  hgvsp: ENSP00000355091.5:p.Gly525Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1634G>A
  hgvsp: ENSP00000423974.2:p.Gly545Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1571G>A
  hgvsp: ENSP00000425765.1:p.Gly524Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1571G>A
  hgvsp: ENSP00000294247.9:p.Gly524Asp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1472G>A
  hgvsp: ENSP00000367041.3:p.Gly491Asp
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly579Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-63672322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672322
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672322
    reference: chr 11
allele count: 2
allele frequency: 1.649076517150396e-5
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1741G>A
  hgvsp: ENSP00000326632.8:p.Ala581Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1579G>A
  hgvsp: ENSP00000355091.5:p.Ala527Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1477G>A
  hgvsp: ENSP00000367041.3:p.Ala493Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1741G>A
  hgvsp: ENSP00000367040.4:p.Ala581Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1501G>A
  hgvsp: ENSP00000415494.2:p.Ala501Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1579G>A
  hgvsp: ENSP00000389184.2:p.Ala527Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1576G>A
  hgvsp: ENSP00000425765.1:p.Ala526Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1738G>A
  hgvsp: ENSP00000423452.3:p.Ala580Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1639G>A
  hgvsp: ENSP00000423974.2:p.Ala547Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1477G>A
  hgvsp: ENSP00000386128.3:p.Ala493Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1642G>A
  hgvsp: ENSP00000421075.2:p.Ala548Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1741G>A
  hgvsp: ENSP00000385751.2:p.Ala581Thr
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1576G>A
  hgvsp: ENSP00000294247.9:p.Ala526Thr
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala581Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

11-63672344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672344
    reference: chr 11
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1763C>T
  hgvsp: ENSP00000385751.2:p.Pro588Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1763C>T
  hgvsp: ENSP00000367040.4:p.Pro588Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1601C>T
  hgvsp: ENSP00000355091.5:p.Pro534Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1601C>T
  hgvsp: ENSP00000389184.2:p.Pro534Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1499C>T
  hgvsp: ENSP00000367041.3:p.Pro500Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1598C>T
  hgvsp: ENSP00000425765.1:p.Pro533Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1661C>T
  hgvsp: ENSP00000423974.2:p.Pro554Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1760C>T
  hgvsp: ENSP00000423452.3:p.Pro587Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1523C>T
  hgvsp: ENSP00000415494.2:p.Pro508Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1598C>T
  hgvsp: ENSP00000294247.9:p.Pro533Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1763C>T
  hgvsp: ENSP00000326632.8:p.Pro588Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1499C>T
  hgvsp: ENSP00000386128.3:p.Pro500Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1664C>T
  hgvsp: ENSP00000421075.2:p.Pro555Leu
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro588Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

11-63672355-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672355
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672355
    reference: chr 11
allele count: 6
allele frequency: 4.947392724034434e-5
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1609T>C
  hgvsp: ENSP00000294247.9:p.Ser537Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1672T>C
  hgvsp: ENSP00000423974.2:p.Ser558Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1612T>C
  hgvsp: ENSP00000389184.2:p.Ser538Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1774T>C
  hgvsp: ENSP00000385751.2:p.Ser592Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1510T>C
  hgvsp: ENSP00000386128.3:p.Ser504Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1675T>C
  hgvsp: ENSP00000421075.2:p.Ser559Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1774T>C
  hgvsp: ENSP00000367040.4:p.Ser592Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1510T>C
  hgvsp: ENSP00000367041.3:p.Ser504Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1771T>C
  hgvsp: ENSP00000423452.3:p.Ser591Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1609T>C
  hgvsp: ENSP00000425765.1:p.Ser537Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1534T>C
  hgvsp: ENSP00000415494.2:p.Ser512Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1774T>C
  hgvsp: ENSP00000326632.8:p.Ser592Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1612T>C
  hgvsp: ENSP00000355091.5:p.Ser538Pro
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser592Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

11-63672357-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672357
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672357
    reference: chr 11
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1776C>T
  hgvsp: ENST00000315032.8:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1773C>T
  hgvsp: ENST00000502399.3:c.1773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1512C>T
  hgvsp: ENST00000377810.3:c.1512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1614C>T
  hgvsp: ENST00000413835.2:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1677C>T
  hgvsp: ENST00000513765.2:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1512C>T
  hgvsp: ENST00000408948.3:c.1512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1536C>T
  hgvsp: ENST00000425897.2:c.1536C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1776C>T
  hgvsp: ENST00000377809.4:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1674C>T
  hgvsp: ENST00000509502.2:c.1674C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1611C>T
  hgvsp: ENST00000350490.7:c.1611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1776C>T
  hgvsp: ENST00000402010.2:c.1776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1611C>T
  hgvsp: ENST00000508192.1:c.1611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1614C>T
  hgvsp: ENST00000361128.5:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser592Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-63672381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672381
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672381
    reference: chr 11
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1701G>A
  hgvsp: ENST00000513765.2:c.1701G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1536G>A
  hgvsp: ENST00000377810.3:c.1536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1638G>A
  hgvsp: ENST00000361128.5:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1638G>A
  hgvsp: ENST00000413835.2:c.1638G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1797G>A
  hgvsp: ENST00000502399.3:c.1797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1800G>A
  hgvsp: ENST00000377809.4:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1536G>A
  hgvsp: ENST00000408948.3:c.1536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1800G>A
  hgvsp: ENST00000315032.8:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1698G>A
  hgvsp: ENST00000509502.2:c.1698G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1635G>A
  hgvsp: ENST00000508192.1:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1560G>A
  hgvsp: ENST00000425897.2:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1635G>A
  hgvsp: ENST00000350490.7:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1800G>A
  hgvsp: ENST00000402010.2:c.1800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly600Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

11-63672385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672385
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672385
    reference: chr 11
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1639C>T
  hgvsp: ENSP00000425765.1:p.Leu547Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1642C>T
  hgvsp: ENSP00000355091.5:p.Leu548Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1540C>T
  hgvsp: ENSP00000386128.3:p.Leu514Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1702C>T
  hgvsp: ENSP00000423974.2:p.Leu568Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1804C>T
  hgvsp: ENSP00000385751.2:p.Leu602Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1642C>T
  hgvsp: ENSP00000389184.2:p.Leu548Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1804C>T
  hgvsp: ENSP00000326632.8:p.Leu602Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1801C>T
  hgvsp: ENSP00000423452.3:p.Leu601Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1564C>T
  hgvsp: ENSP00000415494.2:p.Leu522Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1540C>T
  hgvsp: ENSP00000367041.3:p.Leu514Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1804C>T
  hgvsp: ENSP00000367040.4:p.Leu602Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1639C>T
  hgvsp: ENSP00000294247.9:p.Leu547Phe
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1705C>T
  hgvsp: ENSP00000421075.2:p.Leu569Phe
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu602Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-63672391-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672391
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672391
    reference: chr 11
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1648C>A
  hgvsp: ENSP00000355091.5:p.Gln550Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1648C>A
  hgvsp: ENSP00000389184.2:p.Gln550Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1546C>A
  hgvsp: ENSP00000386128.3:p.Gln516Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1807C>A
  hgvsp: ENSP00000423452.3:p.Gln603Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1810C>A
  hgvsp: ENSP00000326632.8:p.Gln604Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1570C>A
  hgvsp: ENSP00000415494.2:p.Gln524Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1645C>A
  hgvsp: ENSP00000425765.1:p.Gln549Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1810C>A
  hgvsp: ENSP00000367040.4:p.Gln604Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1645C>A
  hgvsp: ENSP00000294247.9:p.Gln549Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1546C>A
  hgvsp: ENSP00000367041.3:p.Gln516Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1711C>A
  hgvsp: ENSP00000421075.2:p.Gln571Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1810C>A
  hgvsp: ENSP00000385751.2:p.Gln604Lys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1708C>A
  hgvsp: ENSP00000423974.2:p.Gln570Lys
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln604Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

11-63672397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672397
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672397
    reference: chr 11
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1717C>T
  hgvsp: ENSP00000421075.2:p.Arg573Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1816C>T
  hgvsp: ENSP00000385751.2:p.Arg606Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1816C>T
  hgvsp: ENSP00000326632.8:p.Arg606Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1576C>T
  hgvsp: ENSP00000415494.2:p.Arg526Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1651C>T
  hgvsp: ENSP00000425765.1:p.Arg551Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1816C>T
  hgvsp: ENSP00000367040.4:p.Arg606Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1813C>T
  hgvsp: ENSP00000423452.3:p.Arg605Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1552C>T
  hgvsp: ENSP00000367041.3:p.Arg518Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1714C>T
  hgvsp: ENSP00000423974.2:p.Arg572Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1654C>T
  hgvsp: ENSP00000389184.2:p.Arg552Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1654C>T
  hgvsp: ENSP00000355091.5:p.Arg552Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1552C>T
  hgvsp: ENSP00000386128.3:p.Arg518Trp
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1651C>T
  hgvsp: ENSP00000294247.9:p.Arg551Trp
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg606Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-63672413-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672413
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672413
    reference: chr 11
allele count: 3
allele frequency: 2.474634991338777e-5
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1832T>C
  hgvsp: ENSP00000385751.2:p.Leu611Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1733T>C
  hgvsp: ENSP00000421075.2:p.Leu578Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1592T>C
  hgvsp: ENSP00000415494.2:p.Leu531Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1832T>C
  hgvsp: ENSP00000326632.8:p.Leu611Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1568T>C
  hgvsp: ENSP00000367041.3:p.Leu523Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1730T>C
  hgvsp: ENSP00000423974.2:p.Leu577Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1667T>C
  hgvsp: ENSP00000294247.9:p.Leu556Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1568T>C
  hgvsp: ENSP00000386128.3:p.Leu523Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1667T>C
  hgvsp: ENSP00000425765.1:p.Leu556Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1670T>C
  hgvsp: ENSP00000355091.5:p.Leu557Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1670T>C
  hgvsp: ENSP00000389184.2:p.Leu557Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1832T>C
  hgvsp: ENSP00000367040.4:p.Leu611Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1829T>C
  hgvsp: ENSP00000423452.3:p.Leu610Ser
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu611Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

11-63672420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672420
    reference: chr 11
allele count: 4
allele frequency: 3.300493423766853e-5
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1839C>T
  hgvsp: ENST00000402010.2:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1677C>T
  hgvsp: ENST00000361128.5:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1575C>T
  hgvsp: ENST00000377810.3:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1575C>T
  hgvsp: ENST00000408948.3:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1839C>T
  hgvsp: ENST00000377809.4:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1836C>T
  hgvsp: ENST00000502399.3:c.1836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1599C>T
  hgvsp: ENST00000425897.2:c.1599C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1839C>T
  hgvsp: ENST00000315032.8:c.1839C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1737C>T
  hgvsp: ENST00000509502.2:c.1737C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1677C>T
  hgvsp: ENST00000413835.2:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1740C>T
  hgvsp: ENST00000513765.2:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1674C>T
  hgvsp: ENST00000508192.1:c.1674C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1674C>T
  hgvsp: ENST00000350490.7:c.1674C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr613Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

11-63672421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672421
    reference: chr 11
allele count: 10
allele frequency: 8.251233559417133e-5
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1675G>A
  hgvsp: ENSP00000425765.1:p.Gly559Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1675G>A
  hgvsp: ENSP00000294247.9:p.Gly559Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1840G>A
  hgvsp: ENSP00000326632.8:p.Gly614Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1678G>A
  hgvsp: ENSP00000389184.2:p.Gly560Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1678G>A
  hgvsp: ENSP00000355091.5:p.Gly560Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1837G>A
  hgvsp: ENSP00000423452.3:p.Gly613Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1840G>A
  hgvsp: ENSP00000367040.4:p.Gly614Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1576G>A
  hgvsp: ENSP00000367041.3:p.Gly526Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1840G>A
  hgvsp: ENSP00000385751.2:p.Gly614Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1576G>A
  hgvsp: ENSP00000386128.3:p.Gly526Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1600G>A
  hgvsp: ENSP00000415494.2:p.Gly534Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1738G>A
  hgvsp: ENSP00000423974.2:p.Gly580Ser
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1741G>A
  hgvsp: ENSP00000421075.2:p.Gly581Ser
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly614Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

11-63672424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672424
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672424
    reference: chr 11
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1678G>A
  hgvsp: ENSP00000294247.9:p.Val560Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1681G>A
  hgvsp: ENSP00000389184.2:p.Val561Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1579G>A
  hgvsp: ENSP00000367041.3:p.Val527Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1741G>A
  hgvsp: ENSP00000423974.2:p.Val581Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1843G>A
  hgvsp: ENSP00000367040.4:p.Val615Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1579G>A
  hgvsp: ENSP00000386128.3:p.Val527Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1843G>A
  hgvsp: ENSP00000326632.8:p.Val615Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1678G>A
  hgvsp: ENSP00000425765.1:p.Val560Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1681G>A
  hgvsp: ENSP00000355091.5:p.Val561Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1843G>A
  hgvsp: ENSP00000385751.2:p.Val615Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1840G>A
  hgvsp: ENSP00000423452.3:p.Val614Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1603G>A
  hgvsp: ENSP00000415494.2:p.Val535Met
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1744G>A
  hgvsp: ENSP00000421075.2:p.Val582Met
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val615Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-63672424-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672424
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672424
    reference: chr 11
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1678G>T
  hgvsp: ENSP00000294247.9:p.Val560Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1603G>T
  hgvsp: ENSP00000415494.2:p.Val535Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1681G>T
  hgvsp: ENSP00000389184.2:p.Val561Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1741G>T
  hgvsp: ENSP00000423974.2:p.Val581Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1843G>T
  hgvsp: ENSP00000326632.8:p.Val615Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1843G>T
  hgvsp: ENSP00000367040.4:p.Val615Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1744G>T
  hgvsp: ENSP00000421075.2:p.Val582Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1678G>T
  hgvsp: ENSP00000425765.1:p.Val560Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1843G>T
  hgvsp: ENSP00000385751.2:p.Val615Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1681G>T
  hgvsp: ENSP00000355091.5:p.Val561Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1579G>T
  hgvsp: ENSP00000367041.3:p.Val527Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1840G>T
  hgvsp: ENSP00000423452.3:p.Val614Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1579G>T
  hgvsp: ENSP00000386128.3:p.Val527Leu
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val615Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-63672427-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672427
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672427
    reference: chr 11
allele count: 3
allele frequency: 2.482046530098951e-5
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1681A>C
  hgvsp: ENSP00000425765.1:p.Thr561Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1582A>C
  hgvsp: ENSP00000367041.3:p.Thr528Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1681A>C
  hgvsp: ENSP00000294247.9:p.Thr561Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1684A>C
  hgvsp: ENSP00000389184.2:p.Thr562Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1744A>C
  hgvsp: ENSP00000423974.2:p.Thr582Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1846A>C
  hgvsp: ENSP00000367040.4:p.Thr616Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1843A>C
  hgvsp: ENSP00000423452.3:p.Thr615Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1747A>C
  hgvsp: ENSP00000421075.2:p.Thr583Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1606A>C
  hgvsp: ENSP00000415494.2:p.Thr536Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1846A>C
  hgvsp: ENSP00000326632.8:p.Thr616Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1846A>C
  hgvsp: ENSP00000385751.2:p.Thr616Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1582A>C
  hgvsp: ENSP00000386128.3:p.Thr528Pro
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1684A>C
  hgvsp: ENSP00000355091.5:p.Thr562Pro
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr616Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

11-63672429-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672429
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672429
    reference: chr 11
allele count: 9
allele frequency: 7.432979303282074e-5
allele num: 121082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1683C>G
  hgvsp: ENST00000508192.1:c.1683C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1683C>G
  hgvsp: ENST00000350490.7:c.1683C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1848C>G
  hgvsp: ENST00000377809.4:c.1848C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1686C>G
  hgvsp: ENST00000413835.2:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1746C>G
  hgvsp: ENST00000509502.2:c.1746C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1584C>G
  hgvsp: ENST00000408948.3:c.1584C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1845C>G
  hgvsp: ENST00000502399.3:c.1845C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1584C>G
  hgvsp: ENST00000377810.3:c.1584C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1848C>G
  hgvsp: ENST00000315032.8:c.1848C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1848C>G
  hgvsp: ENST00000402010.2:c.1848C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1608C>G
  hgvsp: ENST00000425897.2:c.1608C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1686C>G
  hgvsp: ENST00000361128.5:c.1686C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1749C>G
  hgvsp: ENST00000513765.2:c.1749C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr616Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-63672460-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672460
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672460
    reference: chr 11
allele count: 2
allele frequency: 1.660357308892874e-5
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1714C>A
  hgvsp: ENST00000508192.1:c.1714C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1879C>A
  hgvsp: ENST00000315032.8:c.1879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1639C>A
  hgvsp: ENST00000425897.2:c.1639C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1777C>A
  hgvsp: ENST00000509502.2:c.1777C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1717C>A
  hgvsp: ENST00000413835.2:c.1717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1615C>A
  hgvsp: ENST00000408948.3:c.1615C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1780C>A
  hgvsp: ENST00000513765.2:c.1780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1615C>A
  hgvsp: ENST00000377810.3:c.1615C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1879C>A
  hgvsp: ENST00000402010.2:c.1879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1879C>A
  hgvsp: ENST00000377809.4:c.1879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1876C>A
  hgvsp: ENST00000502399.3:c.1876C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1717C>A
  hgvsp: ENST00000361128.5:c.1717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1714C>A
  hgvsp: ENST00000350490.7:c.1714C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg627Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-63672463-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672463
    reference: chr 11
allele count: 3
allele frequency: 2.490949549968448e-5
allele num: 120436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1783C>A
  hgvsp: ENST00000513765.2:c.1783C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1882C>A
  hgvsp: ENST00000377809.4:c.1882C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1780C>A
  hgvsp: ENST00000509502.2:c.1780C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1642C>A
  hgvsp: ENST00000425897.2:c.1642C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1618C>A
  hgvsp: ENST00000377810.3:c.1618C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1882C>A
  hgvsp: ENST00000315032.8:c.1882C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1717C>A
  hgvsp: ENST00000508192.1:c.1717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1879C>A
  hgvsp: ENST00000502399.3:c.1879C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1720C>A
  hgvsp: ENST00000413835.2:c.1720C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1717C>A
  hgvsp: ENST00000350490.7:c.1717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1618C>A
  hgvsp: ENST00000408948.3:c.1618C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1882C>A
  hgvsp: ENST00000402010.2:c.1882C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1720C>A
  hgvsp: ENST00000361128.5:c.1720C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg628Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-63672464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672464
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672464
    reference: chr 11
allele count: 1
allele frequency: 8.302337938363443e-6
allele num: 120448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1721G>A
  hgvsp: ENSP00000389184.2:p.Arg574Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1883G>A
  hgvsp: ENSP00000385751.2:p.Arg628Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1721G>A
  hgvsp: ENSP00000355091.5:p.Arg574Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1718G>A
  hgvsp: ENSP00000425765.1:p.Arg573Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1718G>A
  hgvsp: ENSP00000294247.9:p.Arg573Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1781G>A
  hgvsp: ENSP00000423974.2:p.Arg594Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1883G>A
  hgvsp: ENSP00000326632.8:p.Arg628Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1643G>A
  hgvsp: ENSP00000415494.2:p.Arg548Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1883G>A
  hgvsp: ENSP00000367040.4:p.Arg628Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1880G>A
  hgvsp: ENSP00000423452.3:p.Arg627Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1619G>A
  hgvsp: ENSP00000386128.3:p.Arg540Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1784G>A
  hgvsp: ENSP00000421075.2:p.Arg595Gln
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1619G>A
  hgvsp: ENSP00000367041.3:p.Arg540Gln
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg628Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-63672468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672468
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672468
    reference: chr 11
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1887G>A
  hgvsp: ENST00000315032.8:c.1887G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1722G>A
  hgvsp: ENST00000508192.1:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1725G>A
  hgvsp: ENST00000361128.5:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1887G>A
  hgvsp: ENST00000377809.4:c.1887G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1623G>A
  hgvsp: ENST00000377810.3:c.1623G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1884G>A
  hgvsp: ENST00000502399.3:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1785G>A
  hgvsp: ENST00000509502.2:c.1785G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1722G>A
  hgvsp: ENST00000350490.7:c.1722G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1647G>A
  hgvsp: ENST00000425897.2:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1725G>A
  hgvsp: ENST00000413835.2:c.1725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1887G>A
  hgvsp: ENST00000402010.2:c.1887G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1788G>A
  hgvsp: ENST00000513765.2:c.1788G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1623G>A
  hgvsp: ENST00000408948.3:c.1623G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly629Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-63672479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672479
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672479
    reference: chr 11
allele count: 65
allele frequency: 5.399926893297444e-4
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1796G>A
  hgvsp: ENSP00000423974.2:p.Ser599Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1634G>A
  hgvsp: ENSP00000386128.3:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1733G>A
  hgvsp: ENSP00000294247.9:p.Ser578Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1799G>A
  hgvsp: ENSP00000421075.2:p.Ser600Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1895G>A
  hgvsp: ENSP00000423452.3:p.Ser632Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1898G>A
  hgvsp: ENSP00000326632.8:p.Ser633Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1733G>A
  hgvsp: ENSP00000425765.1:p.Ser578Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1898G>A
  hgvsp: ENSP00000367040.4:p.Ser633Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1736G>A
  hgvsp: ENSP00000389184.2:p.Ser579Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1898G>A
  hgvsp: ENSP00000385751.2:p.Ser633Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1634G>A
  hgvsp: ENSP00000367041.3:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1658G>A
  hgvsp: ENSP00000415494.2:p.Ser553Asn
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1736G>A
  hgvsp: ENSP00000355091.5:p.Ser579Asn
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser633Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

11-63672486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672486
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672486
    reference: chr 11
allele count: 1
allele frequency: 8.311032063961702e-6
allele num: 120322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1905C>T
  hgvsp: ENST00000377809.4:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1641C>T
  hgvsp: ENST00000377810.3:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1641C>T
  hgvsp: ENST00000408948.3:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1743C>T
  hgvsp: ENST00000413835.2:c.1743C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1665C>T
  hgvsp: ENST00000425897.2:c.1665C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1740C>T
  hgvsp: ENST00000508192.1:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1905C>T
  hgvsp: ENST00000402010.2:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1803C>T
  hgvsp: ENST00000509502.2:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1902C>T
  hgvsp: ENST00000502399.3:c.1902C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1743C>T
  hgvsp: ENST00000361128.5:c.1743C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1905C>T
  hgvsp: ENST00000315032.8:c.1905C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1806C>T
  hgvsp: ENST00000513765.2:c.1806C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1740C>T
  hgvsp: ENST00000350490.7:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe635Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

11-63672492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672492
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672492
    reference: chr 11
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1908G>A
  hgvsp: ENST00000502399.3:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1671G>A
  hgvsp: ENST00000425897.2:c.1671G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1749G>A
  hgvsp: ENST00000413835.2:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1911G>A
  hgvsp: ENST00000315032.8:c.1911G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1809G>A
  hgvsp: ENST00000509502.2:c.1809G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1749G>A
  hgvsp: ENST00000361128.5:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1647G>A
  hgvsp: ENST00000377810.3:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1647G>A
  hgvsp: ENST00000408948.3:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1911G>A
  hgvsp: ENST00000377809.4:c.1911G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1911G>A
  hgvsp: ENST00000402010.2:c.1911G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1746G>A
  hgvsp: ENST00000508192.1:c.1746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1746G>A
  hgvsp: ENST00000350490.7:c.1746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1812G>A
  hgvsp: ENST00000513765.2:c.1812G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys637Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-63672495-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672495
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672495
    reference: chr 11
allele count: 6
allele frequency: 4.990767080900334e-5
allele num: 120222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1752C>A
  hgvsp: ENSP00000355091.5:p.Phe584Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1914C>A
  hgvsp: ENSP00000326632.8:p.Phe638Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1752C>A
  hgvsp: ENSP00000389184.2:p.Phe584Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1650C>A
  hgvsp: ENSP00000367041.3:p.Phe550Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1674C>A
  hgvsp: ENSP00000415494.2:p.Phe558Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1815C>A
  hgvsp: ENSP00000421075.2:p.Phe605Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1914C>A
  hgvsp: ENSP00000367040.4:p.Phe638Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1911C>A
  hgvsp: ENSP00000423452.3:p.Phe637Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1812C>A
  hgvsp: ENSP00000423974.2:p.Phe604Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1749C>A
  hgvsp: ENSP00000294247.9:p.Phe583Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1749C>A
  hgvsp: ENSP00000425765.1:p.Phe583Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1914C>A
  hgvsp: ENSP00000385751.2:p.Phe638Leu
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1650C>A
  hgvsp: ENSP00000386128.3:p.Phe550Leu
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe638Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

11-63672495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672495
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672495
    reference: chr 11
allele count: 1
allele frequency: 8.317945134833891e-6
allele num: 120222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1752C>T
  hgvsp: ENST00000413835.2:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1749C>T
  hgvsp: ENST00000350490.7:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1911C>T
  hgvsp: ENST00000502399.3:c.1911C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1650C>T
  hgvsp: ENST00000377810.3:c.1650C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1914C>T
  hgvsp: ENST00000377809.4:c.1914C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1749C>T
  hgvsp: ENST00000508192.1:c.1749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1914C>T
  hgvsp: ENST00000402010.2:c.1914C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1812C>T
  hgvsp: ENST00000509502.2:c.1812C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1752C>T
  hgvsp: ENST00000361128.5:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1914C>T
  hgvsp: ENST00000315032.8:c.1914C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1650C>T
  hgvsp: ENST00000408948.3:c.1650C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1674C>T
  hgvsp: ENST00000425897.2:c.1674C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1815C>T
  hgvsp: ENST00000513765.2:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe638Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

11-63672498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672498
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672498
    reference: chr 11
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1752C>T
  hgvsp: ENST00000508192.1:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1917C>T
  hgvsp: ENST00000377809.4:c.1917C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1818C>T
  hgvsp: ENST00000513765.2:c.1818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1752C>T
  hgvsp: ENST00000350490.7:c.1752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1815C>T
  hgvsp: ENST00000509502.2:c.1815C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1917C>T
  hgvsp: ENST00000402010.2:c.1917C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1677C>T
  hgvsp: ENST00000425897.2:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1917C>T
  hgvsp: ENST00000315032.8:c.1917C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1755C>T
  hgvsp: ENST00000413835.2:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1653C>T
  hgvsp: ENST00000377810.3:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1914C>T
  hgvsp: ENST00000502399.3:c.1914C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1653C>T
  hgvsp: ENST00000408948.3:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1755C>T
  hgvsp: ENST00000361128.5:c.1755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr639Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

11-63672511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672511
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672511
    reference: chr 11
allele count: 1
allele frequency: 8.371142995864656e-6
allele num: 119458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1828C>T
  hgvsp: ENSP00000423974.2:p.Arg610Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1765C>T
  hgvsp: ENSP00000425765.1:p.Arg589Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1927C>T
  hgvsp: ENSP00000423452.3:p.Arg643Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1690C>T
  hgvsp: ENSP00000415494.2:p.Arg564Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1930C>T
  hgvsp: ENSP00000326632.8:p.Arg644Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1666C>T
  hgvsp: ENSP00000367041.3:p.Arg556Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1666C>T
  hgvsp: ENSP00000386128.3:p.Arg556Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1930C>T
  hgvsp: ENSP00000385751.2:p.Arg644Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1930C>T
  hgvsp: ENSP00000367040.4:p.Arg644Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1768C>T
  hgvsp: ENSP00000389184.2:p.Arg590Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1768C>T
  hgvsp: ENSP00000355091.5:p.Arg590Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1831C>T
  hgvsp: ENSP00000421075.2:p.Arg611Cys
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1765C>T
  hgvsp: ENSP00000294247.9:p.Arg589Cys
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg644Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-63672512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672512
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672512
    reference: chr 11
allele count: 2
allele frequency: 1.674593073883047e-5
allele num: 119432
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1931G>A
  hgvsp: ENSP00000385751.2:p.Arg644His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1931G>A
  hgvsp: ENSP00000367040.4:p.Arg644His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1766G>A
  hgvsp: ENSP00000294247.9:p.Arg589His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1667G>A
  hgvsp: ENSP00000367041.3:p.Arg556His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1769G>A
  hgvsp: ENSP00000389184.2:p.Arg590His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1691G>A
  hgvsp: ENSP00000415494.2:p.Arg564His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1766G>A
  hgvsp: ENSP00000425765.1:p.Arg589His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1931G>A
  hgvsp: ENSP00000326632.8:p.Arg644His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1769G>A
  hgvsp: ENSP00000355091.5:p.Arg590His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1832G>A
  hgvsp: ENSP00000421075.2:p.Arg611His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1829G>A
  hgvsp: ENSP00000423974.2:p.Arg610His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1928G>A
  hgvsp: ENSP00000423452.3:p.Arg643His
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1667G>A
  hgvsp: ENSP00000386128.3:p.Arg556His
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg644His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-63672526-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672526
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672526
    reference: chr 11
allele count: 2
allele frequency: 1.687906152417926e-5
allele num: 118490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+11A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+11A>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ

11-63672534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672534
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672534
    reference: chr 11
allele count: 3
allele frequency: 2.545004156840123e-5
allele num: 117878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+19G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+19G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-63672536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672536
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672536
    reference: chr 11
allele count: 2
allele frequency: 1.698398410299088e-5
allele num: 117758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+21G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+21G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

11-63672539-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672539
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672539
    reference: chr 11
allele count: 5
allele frequency: 4.258000783472144e-5
allele num: 117426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+24A>T
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+24A>T
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-63672543-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672543
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672543
    reference: chr 11
allele count: 4
allele frequency: 3.41087386588444e-5
allele num: 117272
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+28A>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+28A>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-63672548-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672548
    reference: chr 11
allele count: 2
allele frequency: 1.715412985676302e-5
allele num: 116590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+33C>G
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+33C>G
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-63672556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672556
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672556
    reference: chr 11
allele count: 1
allele frequency: 8.639905997822744e-6
allele num: 115742
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+41G>A
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+41G>A
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-63672556-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 63672556
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 63672556
    reference: chr 11
allele count: 1
allele frequency: 8.639905997822744e-6
allele num: 115742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000386128
  ensembl transcript: ENST00000408948
  gene symbol: MARK2
  hgvsc: ENST00000408948.3:c.1670+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367041
  ensembl transcript: ENST00000377810
  gene symbol: MARK2
  hgvsc: ENST00000377810.3:c.1670+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423452
  ensembl transcript: ENST00000502399
  gene symbol: MARK2
  hgvsc: ENST00000502399.3:c.1931+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000421075
  ensembl transcript: ENST00000513765
  gene symbol: MARK2
  hgvsc: ENST00000513765.2:c.1835+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000294247
  ensembl transcript: ENST00000350490
  gene symbol: MARK2
  hgvsc: ENST00000350490.7:c.1769+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000367040
  ensembl transcript: ENST00000377809
  gene symbol: MARK2
  hgvsc: ENST00000377809.4:c.1934+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000425765
  ensembl transcript: ENST00000508192
  gene symbol: MARK2
  hgvsc: ENST00000508192.1:c.1769+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000389184
  ensembl transcript: ENST00000413835
  gene symbol: MARK2
  hgvsc: ENST00000413835.2:c.1772+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000326632
  ensembl transcript: ENST00000315032
  gene symbol: MARK2
  hgvsc: ENST00000315032.8:c.1934+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000423974
  ensembl transcript: ENST00000509502
  gene symbol: MARK2
  hgvsc: ENST00000509502.2:c.1832+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000385751
  ensembl transcript: ENST00000402010
  gene symbol: MARK2
  hgvsc: ENST00000402010.2:c.1934+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000355091
  ensembl transcript: ENST00000361128
  gene symbol: MARK2
  hgvsc: ENST00000361128.5:c.1772+41G>C
  variant of: http://identifiers.org/hgnc/3332
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072518
  ensembl protein: ENSP00000415494
  ensembl transcript: ENST00000425897
  gene symbol: MARK2
  hgvsc: ENST00000425897.2:c.1694+41G>C
  variant of: http://identifiers.org/hgnc/3332
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
reference allele: G

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14442
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28014
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2111
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.75e1
variant carriers: 13

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.505808920679758e-4
allele num: 43898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3350
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.41306266548985e-4
allele num: 6798
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

QD
type: SiteQuality
SIO_000300: 1.028e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 9.21346e5

GenotypeDepth
all individuals: 21585
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3005
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32717
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.01256e5

FS
type: SiteQuality
SIO_000300: 2.858e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 3.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.004e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeDepth
all individuals: 0
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4419
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34617
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.928257686676428e-5
allele num: 34150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: -1.697e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.792e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 7.51184e5

QD
type: SiteQuality
SIO_000300: 6.74e0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16149
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8779
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33996
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.514691410094194e-5
allele num: 28452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1866
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.796e0

DP
type: SiteQuality
SIO_000300: 6.55392e5

GenotypeDepth
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12142
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31274
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.27802037845706e-4
allele num: 1374
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

DP
type: SiteQuality
SIO_000300: 5.96351e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 5.37e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.573e0

GenotypeDepth
all individuals: 12395
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 24937
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 13232
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 0
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12890
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2620
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3340
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.977724741447892e-4
allele num: 2514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.517119884361731e-5
allele num: 22138
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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FS
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

Latino
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allele frequency: 5.44069640914037e-4
allele num: 1838
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 5.207248489897938e-4
allele num: 9602
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 8.802816901408451e-5
allele num: 11360
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 1.93e0

InbreedingCoeff
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QD
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MQ
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele num: 8780
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BaseQRankSum
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SIO_000300: -2.176e0

ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 1864
num of homozygotes: 0

South Asian
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allele frequency: 2.959927140255009e-3
allele num: 8784
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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DP
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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South Asian
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VQSLOD
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ReadPosRankSum
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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East Asian
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European (Non-Finnish)
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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DP
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FS
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

Latino
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South Asian
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African
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European (Non-Finnish)
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Other
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East Asian
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15722
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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East Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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DP
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MQ
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InbreedingCoeff
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QD
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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MQ
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QD
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FS
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ReadPosRankSum
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VQSLOD
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DP
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.185975e6

VQSLOD
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FS
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SIO_000300: 2.787e0

ReadPosRankSum
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SIO_000300: 7.02e-1

MQRankSum
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SIO_000300: -6.77e-1

QD
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SIO_000300: 1.225e1

ClippingRankSum
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SIO_000300: -1.063e0

BaseQRankSum
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SIO_000300: -2.294e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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SIO_000300: 1.93e0

MQ
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SIO_000300: 5.856e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.005891547432969e-5
allele num: 66536
num of homozygotes: 0

MQ
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SIO_000300: 5.947e1

MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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SIO_000300: 3.187334e6

FS
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
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SIO_000300: 8.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 2.278e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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BaseQRankSum
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SIO_000300: 9.370000000000001e-1

MQ
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SIO_000300: 5.874e1

ReadPosRankSum
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SIO_000300: -1.05e0

MQRankSum
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SIO_000300: 1.27e0

QD
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SIO_000300: 9.800000000000001e0

DP
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SIO_000300: 3.18884e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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VQSLOD
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FS
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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num of homozygotes: 0

East Asian
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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num of homozygotes: 0

Latino
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African
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European (Non-Finnish)
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allele count: 1
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allele num: 66636
num of homozygotes: 0

South Asian
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ReadPosRankSum
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ClippingRankSum
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DP
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QD
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BaseQRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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DP
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InbreedingCoeff
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European (Non-Finnish)
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DP
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MQ
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MQRankSum
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VQSLOD
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FS
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African
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European (Non-Finnish)
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East Asian
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VQSLOD
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MQRankSum
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MQ
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FS
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DP
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QD
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GenotypeDepth
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East Asian
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.641548565502938e-5
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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DP
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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DP
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VQSLOD
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QD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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African
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Latino
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East Asian
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QD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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South Asian
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MQRankSum
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VQSLOD
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FS
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.8e-3

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 3.473830477072719e-4
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.972e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.00672753483902e-5
allele num: 66592
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 5.85e-1

QD
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SIO_000300: 1.334e1

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
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SIO_000300: -4.68e-1

MQ
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SIO_000300: 5.966e1

DP
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SIO_000300: 3.183509e6

MQRankSum
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SIO_000300: 2.45e-1

BaseQRankSum
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SIO_000300: 1.59e-1

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
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SIO_000300: 3.89e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.646922631680494e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 9
allele frequency: 1.351554287430545e-4
allele num: 66590
num of homozygotes: 0

DP
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MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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SIO_000300: 7.7e-2

ClippingRankSum
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SIO_000300: -2.51e-1

FS
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SIO_000300: 1.924e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

African
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East Asian
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num of homozygotes: 0

Other
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Latino
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num of homozygotes: 0

South Asian
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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VQSLOD
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FS
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DP
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MQ
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 66426
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Latino
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 9
allele frequency: 1.352935870839722e-4
allele num: 66522
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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VQSLOD
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.005213555243633e-4
allele num: 9974
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66286
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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MQ
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SIO_000300: 5.959e1

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508068164681044e-5
allele num: 66310
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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East Asian
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.821e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
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Other
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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African
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East Asian
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 2.596503375454388e-4
allele num: 11554
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European (Non-Finnish)
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allele num: 66326
num of homozygotes: 0

South Asian
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European (Finnish)
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African
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Other
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MQ
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InbreedingCoeff
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QD
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FS
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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African
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East Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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QD
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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DP
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FS
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66288
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European (Finnish)
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Latino
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Other
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African
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East Asian
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South Asian
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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VQSLOD
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FS
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Latino
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African
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DP
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.042102701387199e-5
allele num: 65744
num of homozygotes: 0

Other
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.5761005521828e-5
allele num: 65558
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East Asian
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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FS
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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FS
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65420
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MQ
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QD
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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African
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QD
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MQ
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InbreedingCoeff
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FS
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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DP
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FS
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35693
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0