16-68024025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024025
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024025
    reference: chr 16
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.919G>A
  hgvsp: ENSP00000412549.2:p.Gly307Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.919G>A
  hgvsp: ENSP00000458977.1:p.Gly307Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2169C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.919G>A
  hgvsp: ENSP00000377430.1:p.Gly307Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*84G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.295G>A
  hgvsp: ENSP00000462652.1:p.Gly99Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2169C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3564
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10724
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly307Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

16-68024026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024026
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024026
    reference: chr 16
allele count: 10
allele frequency: 8.24279991427488e-5
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.918C>T
  hgvsp: ENST00000572888.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.294C>T
  hgvsp: ENST00000575510.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2170G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.918C>T
  hgvsp: ENST00000393847.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*83C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.918C>T
  hgvsp: ENST00000412757.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2170G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14535
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23696
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3917
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn306Asn
num of homozygotes: 1
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-68024026-GTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024026
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024023
    reference: chr 16
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.915_917delGAA
  hgvsp: ENSP00000458977.1:p.Lys305del
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.915_917delGAA
  hgvsp: ENSP00000377430.1:p.Lys305del
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.915_917delGAA
  hgvsp: ENSP00000412549.2:p.Lys305del
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.291_293delGAA
  hgvsp: ENSP00000462652.1:p.Lys97del
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2178_-19+2180delTCT
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*80_*82delGAA
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2178_-99+2180delTCT
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10725
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5083
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys305del
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: GTTC
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-68024032-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024032
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024032
    reference: chr 16
allele count: 992
allele frequency: 8.178745156237118e-3
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.912G>T
  hgvsp: ENSP00000412549.2:p.Lys304Asn
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2176C>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.288G>T
  hgvsp: ENSP00000462652.1:p.Lys96Asn
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.912G>T
  hgvsp: ENSP00000458977.1:p.Lys304Asn
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.912G>T
  hgvsp: ENSP00000377430.1:p.Lys304Asn
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*77G>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2176C>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 14486
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 5.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17569
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 4.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 5.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 5042
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8628
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11153
  bin: 9.75e1
  variant carriers: 949
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys304Asn
num of homozygotes: 40
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

16-68024044-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024044
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024044
    reference: chr 16
allele count: 49
allele frequency: 4.045240650540741e-4
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-10G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2188C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-10G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2188C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-10G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-10G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-10G>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17838
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10285
  bin: 9.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

16-68024045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024045
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024045
    reference: chr 16
allele count: 7
allele frequency: 5.779010633379565e-5
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-11C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-11C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-11C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2189G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-11C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2189G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-11C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-68024048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024048
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024048
    reference: chr 16
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2192C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-14G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-14G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-14G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-14G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-14G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2192C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1839
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3923
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

16-68024050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024050
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024050
    reference: chr 16
allele count: 2
allele frequency: 1.651609493451368e-5
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-16T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2194A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2194A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-16T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-16T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-16T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-16T>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10229
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3506
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8598
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

16-68024052-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024052
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024052
    reference: chr 16
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2196T>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-18A>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2196T>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-18A>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-18A>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-18A>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-18A>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17632
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3916
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5039
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

16-68024055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024055
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024055
    reference: chr 16
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-21T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-21T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-21T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-21T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2199A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-21T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2199A>G
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22589
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3906
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8508
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

16-68024073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024073
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024073
    reference: chr 16
allele count: 126
allele frequency: 1.044325829658854e-3
allele num: 120652
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-39G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-39G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-39G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-39G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2217C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-39G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2217C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14233
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4774
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

16-68024081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024081
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024081
    reference: chr 16
allele count: 26
allele frequency: 2.158930499045088e-4
allele num: 120430
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-47A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-47A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-47A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-47A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-47A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2225T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2225T>C
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2940
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3582
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10179
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-68024082-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024082
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024082
    reference: chr 16
allele count: 251
allele frequency: 2.085167893398907e-3
allele num: 120374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2226G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*75-48C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.910-48C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.910-48C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.910-48C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.286-48C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2226G>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 11852
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10557
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 4.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4547
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 6
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

16-68024683-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024683
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024683
    reference: chr 16
allele count: 1
allele frequency: 8.732709235713287e-6
allele num: 114512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+41C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+41C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+41C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+41C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2827G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2827G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+41C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-68024698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024698
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024698
    reference: chr 16
allele count: 1
allele frequency: 8.685833405715278e-6
allele num: 115130
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+26C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2842G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+26C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+26C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2842G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+26C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+26C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42252
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-68024699-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024699
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024699
    reference: chr 16
allele count: 1
allele frequency: 8.681158413778735e-6
allele num: 115192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+25C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2843G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+25C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2843G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+25C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+25C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+25C>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

16-68024703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024703
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024703
    reference: chr 16
allele count: 4
allele frequency: 3.46470333477696e-5
allele num: 115450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2847C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+21G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+21G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+21G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+21G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2847C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+21G>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

16-68024708-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024708
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024708
    reference: chr 16
allele count: 1
allele frequency: 8.630808534143478e-6
allele num: 115864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2852C>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2852C>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+16G>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+16G>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+16G>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+16G>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+16G>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3468
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

16-68024715-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024715
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024715
    reference: chr 16
allele count: 4
allele frequency: 3.418511238355696e-5
allele num: 117010
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+9C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2859G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2859G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+9C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+9C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+9C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+9C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2595
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4175
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

16-68024722-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024722
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024722
    reference: chr 16
allele count: 1
allele frequency: 8.489829184636805e-6
allele num: 117788
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.909+2T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.909+2T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*74+2T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.909+2T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.285+2T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2866A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2866A>G
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4579
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 3.25e1
  variant carriers: 0
hgvs: c.909+2T>C
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-68024732-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024732
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024732
    reference: chr 16
allele count: 11
allele frequency: 9.234540539632969e-5
allele num: 119118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2876G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.277C>A
  hgvsp: ENSP00000462652.1:p.Gln93Lys
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*66C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.901C>A
  hgvsp: ENSP00000458977.1:p.Gln301Lys
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.901C>A
  hgvsp: ENSP00000377430.1:p.Gln301Lys
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2876G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.901C>A
  hgvsp: ENSP00000412549.2:p.Gln301Lys
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5560
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln301Lys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-68024734-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024734
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024733
    reference: chr 16
allele count: 1
allele frequency: 8.374507997655138e-6
allele num: 119410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*63delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.898delC
  hgvsp: ENSP00000377430.1:p.Leu300CysfsTer4
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2880delG
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.898delC
  hgvsp: ENSP00000458977.1:p.Leu300CysfsTer4
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.274delC
  hgvsp: ENSP00000462652.1:p.Leu92CysfsTer4
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.898delC
  hgvsp: ENSP00000412549.2:p.Leu300CysfsTer4
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2880delG
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu300CysfsTer4
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: AG
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

16-68024736-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024736
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024736
    reference: chr 16
allele count: 2
allele frequency: 1.67260441233044e-5
allele num: 119574
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.897C>A
  hgvsp: ENST00000412757.2:c.897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2880G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2880G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.897C>A
  hgvsp: ENST00000572888.1:c.897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.273C>A
  hgvsp: ENST00000575510.1:c.273C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.897C>A
  hgvsp: ENST00000393847.1:c.897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*62C>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5563
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile299Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-68024741-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024741
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024741
    reference: chr 16
allele count: 7
allele frequency: 5.837711617046118e-5
allele num: 119910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2885C>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.892G>T
  hgvsp: ENSP00000377430.1:p.Asp298Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*57G>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.892G>T
  hgvsp: ENSP00000412549.2:p.Asp298Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2885C>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.268G>T
  hgvsp: ENSP00000462652.1:p.Asp90Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.892G>T
  hgvsp: ENSP00000458977.1:p.Asp298Tyr
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2603
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp298Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

16-68024754-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024754
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024754
    reference: chr 16
allele count: 8
allele frequency: 6.624161629543761e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2898C>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.879G>C
  hgvsp: ENST00000393847.1:c.879G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.879G>C
  hgvsp: ENST00000572888.1:c.879G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.879G>C
  hgvsp: ENST00000412757.2:c.879G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*44G>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2898C>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.255G>C
  hgvsp: ENST00000575510.1:c.255G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg293Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-68024755-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024755
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024755
    reference: chr 16
allele count: 6
allele frequency: 4.965243296921549e-5
allele num: 120840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.254G>A
  hgvsp: ENSP00000462652.1:p.Arg85Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.878G>A
  hgvsp: ENSP00000412549.2:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.878G>A
  hgvsp: ENSP00000458977.1:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2899C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.878G>A
  hgvsp: ENSP00000377430.1:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2899C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg293Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

16-68024756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024756
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024756
    reference: chr 16
allele count: 2
allele frequency: 1.653876686954221e-5
allele num: 120928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2900G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.877C>T
  hgvsp: ENSP00000458977.1:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.877C>T
  hgvsp: ENSP00000377430.1:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.877C>T
  hgvsp: ENSP00000412549.2:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*42C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.253C>T
  hgvsp: ENSP00000462652.1:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2900G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42247
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg293Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-68024766-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024766
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024766
    reference: chr 16
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.867C>A
  hgvsp: ENSP00000412549.2:p.Cys289Ter
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*32C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.867C>A
  hgvsp: ENSP00000458977.1:p.Cys289Ter
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2910G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.867C>A
  hgvsp: ENSP00000377430.1:p.Cys289Ter
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.243C>A
  hgvsp: ENSP00000462652.1:p.Cys81Ter
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2910G>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42248
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6730
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys289Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-68024776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024776
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024776
    reference: chr 16
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.233G>A
  hgvsp: ENSP00000462652.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.857G>A
  hgvsp: ENSP00000377430.1:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2920C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.857G>A
  hgvsp: ENSP00000412549.2:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.857G>A
  hgvsp: ENSP00000458977.1:p.Arg286Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2920C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg286Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-68024777-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024777
    reference: chr 16
allele count: 3
allele frequency: 2.473614775725594e-5
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2921G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.856C>T
  hgvsp: ENSP00000377430.1:p.Arg286Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2921G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.856C>T
  hgvsp: ENSP00000412549.2:p.Arg286Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.232C>T
  hgvsp: ENSP00000462652.1:p.Arg78Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.856C>T
  hgvsp: ENSP00000458977.1:p.Arg286Trp
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg286Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff

16-68024777-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024777
    reference: chr 16
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2921G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.856C>G
  hgvsp: ENSP00000458977.1:p.Arg286Gly
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.856C>G
  hgvsp: ENSP00000377430.1:p.Arg286Gly
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.232C>G
  hgvsp: ENSP00000462652.1:p.Arg78Gly
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*21C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.856C>G
  hgvsp: ENSP00000412549.2:p.Arg286Gly
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2921G>C
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6804
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2609
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg286Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-68024781-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024781
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024781
    reference: chr 16
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2925A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.228T>C
  hgvsp: ENST00000575510.1:c.228T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.852T>C
  hgvsp: ENST00000393847.1:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.852T>C
  hgvsp: ENST00000412757.2:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.852T>C
  hgvsp: ENST00000572888.1:c.852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2925A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*17T>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala284Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

16-68024784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024784
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024784
    reference: chr 16
allele count: 25
allele frequency: 2.06073395100399e-4
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.849G>A
  hgvsp: ENST00000412757.2:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.849G>A
  hgvsp: ENST00000572888.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.849G>A
  hgvsp: ENST00000393847.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.225G>A
  hgvsp: ENST00000575510.1:c.225G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2928C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2928C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42248
  bin: 9.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser283Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

16-68024793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024793
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024793
    reference: chr 16
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.840C>T
  hgvsp: ENST00000393847.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.840C>T
  hgvsp: ENST00000412757.2:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2937G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*5C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.840C>T
  hgvsp: ENST00000572888.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.216C>T
  hgvsp: ENST00000575510.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2937G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42244
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe280Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

16-68024794-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024794
    reference: chr 16
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2938A>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.839T>A
  hgvsp: ENSP00000377430.1:p.Phe280Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.839T>A
  hgvsp: ENSP00000412549.2:p.Phe280Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2938A>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.839T>A
  hgvsp: ENSP00000458977.1:p.Phe280Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.215T>A
  hgvsp: ENSP00000462652.1:p.Phe72Tyr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.*4T>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42244
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe280Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-68024804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024804
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024804
    reference: chr 16
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.829C>T
  hgvsp: ENSP00000412549.2:p.Pro277Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.481C>T
  hgvsp: ENSP00000463604.1:p.Pro161Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.771C>T
  hgvsp: ENST00000575203.1:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2948G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.205C>T
  hgvsp: ENSP00000462652.1:p.Pro69Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.829C>T
  hgvsp: ENSP00000458977.1:p.Pro277Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.829C>T
  hgvsp: ENSP00000377430.1:p.Pro277Ser
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2948G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro277Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

16-68024807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024807
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024807
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.202G>A
  hgvsp: ENSP00000462652.1:p.Ala68Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.826G>A
  hgvsp: ENSP00000412549.2:p.Ala276Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.826G>A
  hgvsp: ENSP00000458977.1:p.Ala276Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.768G>A
  hgvsp: ENST00000575203.1:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.478G>A
  hgvsp: ENSP00000463604.1:p.Ala160Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2951C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.826G>A
  hgvsp: ENSP00000377430.1:p.Ala276Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2951C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala276Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-68024808-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024808
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024808
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.477G>A
  hgvsp: ENST00000573808.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.825G>A
  hgvsp: ENST00000393847.1:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.825G>A
  hgvsp: ENST00000572888.1:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.825G>A
  hgvsp: ENST00000412757.2:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2952C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.767G>A
  hgvsp: ENSP00000459375.1:p.Arg256Lys
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.201G>A
  hgvsp: ENST00000575510.1:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2952C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6868
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg256Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

16-68024826-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024826
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024826
    reference: chr 16
allele count: 4
allele frequency: 3.296522169111587e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.807G>A
  hgvsp: ENST00000393847.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2970C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.807G>A
  hgvsp: ENST00000572888.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2970C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.459G>A
  hgvsp: ENST00000573808.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.183G>A
  hgvsp: ENST00000575510.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.749G>A
  hgvsp: ENSP00000459375.1:p.Gly250Glu
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.807G>A
  hgvsp: ENST00000412757.2:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly250Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

16-68024827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024827
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024827
    reference: chr 16
allele count: 9
allele frequency: 7.417174880501072e-5
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.748G>A
  hgvsp: ENSP00000459375.1:p.Gly250Arg
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2971C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.182G>A
  hgvsp: ENSP00000462652.1:p.Arg61Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.806G>A
  hgvsp: ENSP00000458977.1:p.Arg269Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.458G>A
  hgvsp: ENSP00000463604.1:p.Arg153Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.806G>A
  hgvsp: ENSP00000412549.2:p.Arg269Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.806G>A
  hgvsp: ENSP00000377430.1:p.Arg269Gln
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2971C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg269Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-68024828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024828
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024828
    reference: chr 16
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.805C>T
  hgvsp: ENSP00000412549.2:p.Arg269Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2972G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.747C>T
  hgvsp: ENST00000575203.1:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.805C>T
  hgvsp: ENSP00000377430.1:p.Arg269Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.805C>T
  hgvsp: ENSP00000458977.1:p.Arg269Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2972G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.457C>T
  hgvsp: ENSP00000463604.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.181C>T
  hgvsp: ENSP00000462652.1:p.Arg61Trp
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6846
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg269Trp
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-68024831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024831
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024831
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.178C>T
  hgvsp: ENSP00000462652.1:p.Arg60Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.802C>T
  hgvsp: ENSP00000458977.1:p.Arg268Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2975G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.454C>T
  hgvsp: ENSP00000463604.1:p.Arg152Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.802C>T
  hgvsp: ENSP00000377430.1:p.Arg268Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.744C>T
  hgvsp: ENST00000575203.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.802C>T
  hgvsp: ENSP00000412549.2:p.Arg268Trp
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2975G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg268Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

16-68024849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024849
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024849
    reference: chr 16
allele count: 8
allele frequency: 6.593805120089676e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.436G>A
  hgvsp: ENSP00000463604.1:p.Val146Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2993C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-7G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.784G>A
  hgvsp: ENSP00000412549.2:p.Val262Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.784G>A
  hgvsp: ENSP00000377430.1:p.Val262Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2993C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.160G>A
  hgvsp: ENSP00000462652.1:p.Val54Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.784G>A
  hgvsp: ENSP00000458977.1:p.Val262Ile
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3741
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val262Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

16-68024850-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024850
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024850
    reference: chr 16
allele count: 2962
allele frequency: 2.441316101806673e-2
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.783T>C
  hgvsp: ENST00000393847.1:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.435T>C
  hgvsp: ENST00000573808.1:c.435T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.783T>C
  hgvsp: ENST00000412757.2:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.783T>C
  hgvsp: ENST00000572888.1:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-8T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2994A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2994A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.159T>C
  hgvsp: ENST00000575510.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 8.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 9.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 9.75e1
  variant carriers: 2089
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 5.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 5.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 4.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 8.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 7.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 6.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 7.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6443
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: c.733-8T>C
num of homozygotes: 201
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-68024853-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024853
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024853
    reference: chr 16
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.432C>G
  hgvsp: ENST00000573808.1:c.432C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.780C>G
  hgvsp: ENST00000393847.1:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.780C>G
  hgvsp: ENST00000412757.2:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+2997G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.156C>G
  hgvsp: ENST00000575510.1:c.156C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.780C>G
  hgvsp: ENST00000572888.1:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-11C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+2997G>C
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41984
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser260Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

16-68024866-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024866
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024866
    reference: chr 16
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3010A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.767T>C
  hgvsp: ENSP00000412549.2:p.Met256Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.143T>C
  hgvsp: ENSP00000462652.1:p.Met48Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.767T>C
  hgvsp: ENSP00000458977.1:p.Met256Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-24T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3010A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.419T>C
  hgvsp: ENSP00000463604.1:p.Met140Thr
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.767T>C
  hgvsp: ENSP00000377430.1:p.Met256Thr
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6394
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met256Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

16-68024870-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024870
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024870
    reference: chr 16
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3014T>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3014T>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.763A>C
  hgvsp: ENSP00000458977.1:p.Met255Leu
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.139A>C
  hgvsp: ENSP00000462652.1:p.Met47Leu
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.415A>C
  hgvsp: ENSP00000463604.1:p.Met139Leu
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.763A>C
  hgvsp: ENSP00000377430.1:p.Met255Leu
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-28A>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.763A>C
  hgvsp: ENSP00000412549.2:p.Met255Leu
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41984
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met255Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

16-68024878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024878
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024878
    reference: chr 16
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.131G>A
  hgvsp: ENSP00000462652.1:p.Arg44His
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3022C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.755G>A
  hgvsp: ENSP00000377430.1:p.Arg252His
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.407G>A
  hgvsp: ENSP00000463604.1:p.Arg136His
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.755G>A
  hgvsp: ENSP00000412549.2:p.Arg252His
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.755G>A
  hgvsp: ENSP00000458977.1:p.Arg252His
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-36G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3022C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg252His
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-68024883-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024883
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024883
    reference: chr 16
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.126G>T
  hgvsp: ENSP00000462652.1:p.Met42Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.750G>T
  hgvsp: ENSP00000412549.2:p.Met250Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.750G>T
  hgvsp: ENSP00000377430.1:p.Met250Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.750G>T
  hgvsp: ENSP00000458977.1:p.Met250Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3027C>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.402G>T
  hgvsp: ENSP00000463604.1:p.Met134Ile
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3027C>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-41G>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met250Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

16-68024898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024898
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024898
    reference: chr 16
allele count: 2
allele frequency: 1.649538953862396e-5
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3042C>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.387G>A
  hgvsp: ENST00000573808.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-56G>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.111G>A
  hgvsp: ENST00000575510.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.735G>A
  hgvsp: ENST00000412757.2:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.735G>A
  hgvsp: ENST00000393847.1:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.735G>A
  hgvsp: ENST00000572888.1:c.735G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3042C>T
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41978
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
hgvs: c.735G>A
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: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-68024902-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024902
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024902
    reference: chr 16
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3046T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-2A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3046T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-2A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-2A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-60A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-2A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-2A>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41977
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
hgvs: c.733-2A>G
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

16-68024903-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024903
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024903
    reference: chr 16
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-3C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-3C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-3C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3047G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3047G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-3C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-3C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-61C>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5537
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
hgvs: c.733-3C>G
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-68024912-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024912
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024912
    reference: chr 16
allele count: 4
allele frequency: 3.299404457495422e-5
allele num: 121234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3056T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-12A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-12A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3056T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-12A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-12A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-12A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-70A>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7094
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-68024920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024920
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024920
    reference: chr 16
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3064G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-20C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-20C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-78C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-20C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3064G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-20C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-20C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5426
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-68024923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024923
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024923
    reference: chr 16
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3067G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3067G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-81C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.75e1
  variant carriers: 0
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: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

16-68024926-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024926
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024926
    reference: chr 16
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3070T>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-26A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-26A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-26A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-26A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-84A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-26A>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3070T>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41973
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-68024927-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024927
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024927
    reference: chr 16
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3071A>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.733-85T>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3071A>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-27T>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-27T>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-27T>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-27T>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-27T>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/16-68024929-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024929
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024928
    reference: chr 16
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+88delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3074delA
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-30delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-30delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-30delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-30delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-30delT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3074delA
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: CA
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-68024929-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024929
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024927
    reference: chr 16
allele count: 5
allele frequency: 4.125821038386639e-5
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-31_733-30delCT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-31_385-30delCT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-31_733-30delCT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-31_109-30delCT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-31_733-30delCT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3074_-19+3075delAG
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3074_-99+3075delAG
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+87_732+88delCT
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: CAG
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-68024933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024933
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024933
    reference: chr 16
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-33C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-33C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+85C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-33C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-33C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3077G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-33C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3077G>A
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41982
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

16-68024936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024936
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024936
    reference: chr 16
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-36C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3080G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+82C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3080G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-36C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-36C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-36C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-36C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-68024941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024941
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024941
    reference: chr 16
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-41A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-41A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-41A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3085T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3085T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-41A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-41A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+77A>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7084
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5346
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

16-68024946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024946
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024946
    reference: chr 16
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3090A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-46T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-46T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-46T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3090A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-46T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+72T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-46T>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-68024950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024950
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024950
    reference: chr 16
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+68T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.733-50T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.109-50T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.733-50T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3094A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.385-50T>C
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3094A>G
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.733-50T>C
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-68024974-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024974
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024974
    reference: chr 16
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+44C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3118G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+44C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+44C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+44C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3118G>T
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+44C>A
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+44C>A
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

16-68024975-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024975
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024975
    reference: chr 16
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+43A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3119T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+43A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+43A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+43A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+43A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3119T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+43A>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15843
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

16-68024981-CATTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024981
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024977
    reference: chr 16
allele count: 5
allele frequency: 4.120516877637131e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+33_384+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+33_732+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+33_732+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3126_-19+3129delATTT
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+33_732+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+33_108+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+33_732+36delAAAT
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3126_-99+3129delATTT
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: CATTT
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-68024984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024984
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024984
    reference: chr 16
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3128T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+34A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3128T>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+34A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+34A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+34A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+34A>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+34A>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28669
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15827
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-68024989-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024989
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024988
    reference: chr 16
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3137delG
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+28delC
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3137delG
  variant of: http://identifiers.org/hgnc/26014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TG
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-68024995-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024995
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024995
    reference: chr 16
allele count: 20541
allele frequency: 1.693544397724462e-1
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3139G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3139G>A
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+23C>T
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+23C>T
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 7.25e1
  variant carriers: 912
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.75e1
  variant carriers: 631
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 2377
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 8.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.75e1
  variant carriers: 2110
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 2.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 21746
  bin: 2.75e1
  variant carriers: 358
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.75e1
  variant carriers: 1498
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 6.25e1
  variant carriers: 1663
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 9.75e1
  variant carriers: 1442
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 3.25e1
  variant carriers: 921
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 4.75e1
  variant carriers: 2316
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 6.75e1
  variant carriers: 1219
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 4.25e1
  variant carriers: 2085
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 8.25e1
  variant carriers: 460
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.25e1
  variant carriers: 217
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5797
  bin: 6.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 8.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 7.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 5
num of homozygotes: 1861
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-68024996-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68024996
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68024996
    reference: chr 16
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000461244
  ensembl transcript: ENST00000570709
  gene symbol: DUS2
  hgvsc: ENST00000570709.2:c.-19+3140G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000462652
  ensembl transcript: ENST00000575510
  gene symbol: DPEP2
  hgvsc: ENST00000575510.1:c.108+22C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000463604
  ensembl transcript: ENST00000573808
  gene symbol: DPEP2
  hgvsc: ENST00000573808.1:c.384+22C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000458977
  ensembl transcript: ENST00000572888
  gene symbol: DPEP2
  hgvsc: ENST00000572888.1:c.732+22C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000377430
  ensembl transcript: ENST00000393847
  gene symbol: DPEP2
  hgvsc: ENST00000393847.1:c.732+22C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000412549
  ensembl transcript: ENST00000412757
  gene symbol: DPEP2
  hgvsc: ENST00000412757.2:c.732+22C>G
  variant of: http://identifiers.org/hgnc/23028
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167264
  ensembl protein: ENSP00000458906
  ensembl transcript: ENST00000571081
  gene symbol: DUS2
  hgvsc: ENST00000571081.2:c.-99+3140G>C
  variant of: http://identifiers.org/hgnc/26014
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167261
  ensembl protein: ENSP00000459375
  ensembl transcript: ENST00000575203
  gene symbol: DPEP2
  hgvsc: ENST00000575203.1:c.732+22C>G
  variant of: http://identifiers.org/hgnc/23028
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3931
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5089
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.102421e6

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10725
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.157407407407407e-3
allele num: 8640
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.94e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

DP
type: SiteQuality
SIO_000300: 2.102097e6

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.559e1

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 1.499e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
all individuals: 1847
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 8701
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3917
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variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.559e1

DP
type: SiteQuality
SIO_000300: 2.102097e6

FS
type: SiteQuality
SIO_000300: 1.499e0

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 9.25e1
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GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3895
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variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 976
allele frequency: 5.918020858598108e-2
allele num: 16492
num of homozygotes: 40

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.456022118541559e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499640028797696e-5
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.35e-2

DP
type: SiteQuality
SIO_000300: 2.112034e6

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

QD
type: SiteQuality
SIO_000300: 1.383e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.219e0

GenotypeQuality
all individuals: 2928
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5071
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 23424
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variant carriers: 0

GenotypeQuality
all individuals: 3938
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 8654
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.806248122559327e-4
allele num: 66580
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 7.295719844357977e-4
allele num: 16448
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.429e1

DP
type: SiteQuality
SIO_000300: 2.075924e6

GenotypeQuality
all individuals: 8658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2924
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 5071
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10246
bin: 9.75e1
variant carriers: 7

South Asian
type: Population
allele count: 6
allele frequency: 3.64741641337386e-4
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

FS
type: SiteQuality
SIO_000300: 7.695e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.506e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 2.073316e6

GenotypeQuality
all individuals: 2912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5048
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 466
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 10230
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.961e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 6.461e0

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.068764e6

QD
type: SiteQuality
SIO_000300: 1.093e1

GenotypeQuality
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 494
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GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 2911
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variant carriers: 0

GenotypeQuality
all individuals: 5046
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005168890491646e-5
allele num: 66552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 2.066953e6

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.244e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.722e1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 219
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GenotypeQuality
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GenotypeQuality
all individuals: 256
bin: 2.75e1
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GenotypeQuality
all individuals: 2908
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GenotypeQuality
all individuals: 22934
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variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10226
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.093e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

QD
type: SiteQuality
SIO_000300: 7.13e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.063242e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

GenotypeQuality
all individuals: 309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
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GenotypeQuality
all individuals: 3488
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5025
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GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.612e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

QD
type: SiteQuality
SIO_000300: 1.212e1

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.057404e6

GenotypeQuality
all individuals: 693
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
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GenotypeQuality
all individuals: 16446
bin: 6.25e1
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GenotypeQuality
all individuals: 1385
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GenotypeQuality
all individuals: 2097
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GenotypeQuality
all individuals: 1868
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GenotypeQuality
all individuals: 970
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GenotypeQuality
all individuals: 10275
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variant carriers: 126

GenotypeQuality
all individuals: 2870
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variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.465003465003465e-4
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.056221142529499e-4
allele num: 66274
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 113
allele frequency: 1.089891975308642e-2
allele num: 10368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.443e0

VQSLOD
type: SiteQuality
SIO_000300: 5.87e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.973535e6

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.3e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3752
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
type: Population
allele count: 26
allele frequency: 2.255378209576683e-3
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.940532e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.274e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 243

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

African
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allele count: 8
allele frequency: 7.729468599033816e-4
allele num: 10350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 227
allele frequency: 3.433982814958248e-3
allele num: 66104
num of homozygotes: 6

Other
type: Population
allele count: 3
allele frequency: 3.34075723830735e-3
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.128864188954498e-3
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.13e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.939728e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.659e0

QD
type: SiteQuality
SIO_000300: 1.442e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544067691927614e-5
allele num: 64764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -3.093e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

FS
type: SiteQuality
SIO_000300: 1.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

DP
type: SiteQuality
SIO_000300: 3.203194e6

QD
type: SiteQuality
SIO_000300: 1.488e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.906e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 430
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539882968894364e-5
allele num: 64940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12316
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.6327e1

VQSLOD
type: SiteQuality
SIO_000300: -1.591e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.63e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 3.21288e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.845e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
all individuals: 389
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 670
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 1523
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 734
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GenotypeQuality
all individuals: 943
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539456264047538e-5
allele num: 64958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12358
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 3.213916e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.3e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.237e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.357e1

GenotypeQuality
all individuals: 626
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 42255
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variant carriers: 4

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.194377894904967e-4
allele num: 12522
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.957e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

MQ
type: SiteQuality
SIO_000300: 5.789e1

DP
type: SiteQuality
SIO_000300: 3.217706e6

GenotypeQuality
all individuals: 2107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 2593
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
type: Population
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: 8632
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 3.224157e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

FS
type: SiteQuality
SIO_000300: 5.632e0

MQ
type: SiteQuality
SIO_000300: 5.737e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.05548765582987e-5
allele num: 65456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.18e-2

MQ
type: SiteQuality
SIO_000300: 5.822e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.363e-1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

South Asian
type: Population
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: 8638
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: 862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523043650431021e-5
allele num: 65658
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.881e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2600
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GenotypeQuality
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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: 11

GenotypeQuality
all individuals: 249
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GenotypeQuality
all individuals: 2150
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
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Latino
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allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
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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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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 (Non-Finnish)
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allele count: 10
allele frequency: 1.514784294716432e-4
allele num: 66016
num of homozygotes: 0

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

QD
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -7.42e-1

DP
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VQSLOD
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MQRankSum
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SIO_000300: -9.3e-2

MQ
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SIO_000300: 5.829e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1928
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variant carriers: 0

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

African
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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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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: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

East Asian
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allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.333e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8642
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.30582397492818e-4
allele num: 15316
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

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

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 3.263413e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

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

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

Other
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allele frequency: 0.0e0
allele num: 892
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: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.056284895126e-4
allele num: 66270
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.2e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.942e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 1.106e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 3.268451e6

VQSLOD
type: SiteQuality
SIO_000300: -5.845e-1

MQ
type: SiteQuality
SIO_000300: 5.861e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 64
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66504
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 8
allele frequency: 9.248554913294797e-4
allele num: 8650
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQ
type: SiteQuality
SIO_000300: 5.892e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

DP
type: SiteQuality
SIO_000300: 3.278772e6

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
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: 3.006253006253006e-5
allele num: 66528
num of homozygotes: 0

African
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allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

Latino
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allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.109e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.93e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.9e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele frequency: 3.004897983713453e-5
allele num: 66558
num of homozygotes: 0

African
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Other
type: Population
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South Asian
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East Asian
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FS
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66622
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European (Finnish)
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allele count: 0
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Latino
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South Asian
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Other
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ClippingRankSum
type: SiteQuality
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FS
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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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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Other
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BaseQRankSum
type: SiteQuality
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MQ
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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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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variant carriers: 0

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

Other
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 4.500855162480871e-5
allele num: 66654
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Latino
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African
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.88e1

DP
type: SiteQuality
SIO_000300: 3.285121e6

QD
type: SiteQuality
SIO_000300: 1.311e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.029e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

FS
type: SiteQuality
SIO_000300: 2.493e0

DP
type: SiteQuality
SIO_000300: 3.285121e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 5.88e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

GenotypeQuality
all individuals: 42245
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1122
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1966
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GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.101e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 3.284858e6

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

GenotypeQuality
all individuals: 6832
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
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variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1121
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.449931001379972e-4
allele num: 66668
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

DP
type: SiteQuality
SIO_000300: 3.285995e6

MQ
type: SiteQuality
SIO_000300: 5.879e1

VQSLOD
type: SiteQuality
SIO_000300: 7.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.407e1

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6857
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
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variant carriers: 0

GenotypeQuality
all individuals: 1125
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variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.904e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 5.897e1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 3.283405e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.232e0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2231
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1971
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variant carriers: 0

GenotypeQuality
all individuals: 6873
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variant carriers: 0

GenotypeQuality
all individuals: 2611
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 1.014e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

DP
type: SiteQuality
SIO_000300: 3.283444e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.694e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.441e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
all individuals: 2613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1127
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 1977
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42245
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
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: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.208e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.283556e6

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.85e-1

FS
type: SiteQuality
SIO_000300: 7.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 42246
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 1.042e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.607e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 3.283608e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2613
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 3.283585e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.58e-1

FS
type: SiteQuality
SIO_000300: 3.371e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.753e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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

GenotypeQuality
all individuals: 42238
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1135
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 2193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.75e1
variant carriers: 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
allele num: 16498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.998260504453708e-5
allele num: 66686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.280171e6

QD
type: SiteQuality
SIO_000300: 1.146e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.592e0

FS
type: SiteQuality
SIO_000300: 2.533e0

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.193e0

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1984
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variant carriers: 0

GenotypeQuality
all individuals: 2193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6830
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049695588279399e-4
allele num: 66686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 3.279913e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.182e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.685e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 1.435e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.845e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.395e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e0

DP
type: SiteQuality
SIO_000300: 3.279074e6

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 1987
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variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.575e0

DP
type: SiteQuality
SIO_000300: 3.27891e6

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2196
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variant carriers: 0

GenotypeQuality
all individuals: 1982
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variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.853779881082393e-4
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.278158e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.905e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.805e-1

FS
type: SiteQuality
SIO_000300: 1.907e0

QD
type: SiteQuality
SIO_000300: 1.643e1

MQRankSum
type: SiteQuality
SIO_000300: -4.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 42777
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variant carriers: 2757

GenotypeQuality
all individuals: 6
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1319
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2596
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GenotypeQuality
all individuals: 1101
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 17
allele frequency: 1.872246696035242e-2
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 144
allele frequency: 1.24373812402833e-2
allele num: 11578
num of homozygotes: 1

African
type: Population
allele count: 2017
allele frequency: 1.938677431757017e-1
allele num: 10404
num of homozygotes: 189

East Asian
type: Population
allele count: 12
allele frequency: 1.386642015253062e-3
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 513
allele frequency: 3.112864077669903e-2
allele num: 16480
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 258
allele frequency: 3.868645973909132e-3
allele num: 66690
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

DP
type: SiteQuality
SIO_000300: 3.337282e6

VQSLOD
type: SiteQuality
SIO_000300: 4.31e0

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.212e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

QD
type: SiteQuality
SIO_000300: 1.491e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 2731
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.068e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.441e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 3.123053e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 41983
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 2.652e0

DP
type: SiteQuality
SIO_000300: 3.121516e6

QD
type: SiteQuality
SIO_000300: 1.378e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 175
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GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2011
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variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.214624073849144e-4
allele num: 16466
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

QD
type: SiteQuality
SIO_000300: 1.525e1

VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 3.120564e6

GenotypeQuality
all individuals: 2266
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 41979
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GenotypeQuality
all individuals: 124
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 1389
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GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 2004
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variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.72e-1

DP
type: SiteQuality
SIO_000300: 3.119629e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.175e0

FS
type: SiteQuality
SIO_000300: 1.804e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.294e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41979
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.465e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.934e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 2.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.118735e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 7.226e0

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

DP
type: SiteQuality
SIO_000300: 3.11794e6

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1163
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variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.11693e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.345e0

FS
type: SiteQuality
SIO_000300: 1.821e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-2

QD
type: SiteQuality
SIO_000300: 9.92e0

GenotypeQuality
all individuals: 2280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087909411907951e-5
allele num: 16426
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: -2.095e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.745e0

QD
type: SiteQuality
SIO_000300: 1.844e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 3.11695e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500855162480871e-5
allele num: 66654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.833e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: -1.117e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.116671e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1180
bin: 7.25e1
variant carriers: 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: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.862e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.993e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.805e0

ReadPosRankSum
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SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQ
type: SiteQuality
SIO_000300: 5.857e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
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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
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.916e1

FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2246
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
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
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

Latino
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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
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

FS
type: SiteQuality
SIO_000300: 2.419e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 3.116006e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2730
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

FS
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.807e1

DP
type: SiteQuality
SIO_000300: 3.115932e6

MQ
type: SiteQuality
SIO_000300: 6.051e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.393e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

East Asian
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allele count: 4
allele frequency: 4.623208506703652e-4
allele num: 8652
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQ
type: SiteQuality
SIO_000300: 6.051e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.94e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.807e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.393e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

DP
type: SiteQuality
SIO_000300: 3.115932e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.919e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.1214e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.97e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 6.57e0

MQRankSum
type: SiteQuality
SIO_000300: -1.065e0

DP
type: SiteQuality
SIO_000300: 3.116078e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.294e1

FS
type: SiteQuality
SIO_000300: 1.2177e1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 3.115899e6

VQSLOD
type: SiteQuality
SIO_000300: -1.447e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.225e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

FS
type: SiteQuality
SIO_000300: 3.393e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.115715e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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 (Non-Finnish)
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allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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allele num: 8650
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 2.251885e6

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 2.914e1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

FS
type: SiteQuality
SIO_000300: 1.271e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 2584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15830
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1892
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996462087368453e-5
allele num: 66706
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.251864e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 9.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

MQ
type: SiteQuality
SIO_000300: 5.617e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.748e0

QD
type: SiteQuality
SIO_000300: 9.69e0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

DP
type: SiteQuality
SIO_000300: 2.251361e6

VQSLOD
type: SiteQuality
SIO_000300: -3.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.013e0

QD
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15828
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1898
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.0e-2

DP
type: SiteQuality
SIO_000300: 2.251634e6

FS
type: SiteQuality
SIO_000300: 1.185e0

MQ
type: SiteQuality
SIO_000300: 6.012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 28203
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 482
bin: 9.25e1
variant carriers: 35

GenotypeQuality
all individuals: 396
bin: 8.75e1
variant carriers: 21

GenotypeQuality
all individuals: 1551
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 21076
bin: 9.75e1
variant carriers: 18494

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 3

African
type: Population
allele count: 2341
allele frequency: 2.251827626010004e-1
allele num: 10396
num of homozygotes: 268

East Asian
type: Population
allele count: 1002
allele frequency: 1.159185562239704e-1
allele num: 8644
num of homozygotes: 62

South Asian
type: Population
allele count: 3523
allele frequency: 2.133858267716535e-1
allele num: 16510
num of homozygotes: 430

Latino
type: Population
allele count: 2029
allele frequency: 1.757623007623008e-1
allele num: 11544
num of homozygotes: 192

European (Non-Finnish)
type: Population
allele count: 10263
allele frequency: 1.53904984703977e-1
allele num: 66684
num of homozygotes: 785

Other
type: Population
allele count: 148
allele frequency: 1.63355408388521e-1
allele num: 906
num of homozygotes: 13

European (Finnish)
type: Population
allele count: 1235
allele frequency: 1.869512564335453e-1
allele num: 6606
num of homozygotes: 111

DP
type: SiteQuality
SIO_000300: 2.410195e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

FS
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.568e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.581e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

GenotypeQuality
all individuals: 1382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40565
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.840303e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1