16-15973626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973626
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973626
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 52236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4239G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4239G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+35G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+35G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26688
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

16-15973628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973628
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973628
    reference: chr 16
allele count: 4486
allele frequency: 8.113289445127686e-2
allele num: 55292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4237T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+33T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4237T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+33T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 1.75e1
  variant carriers: 915
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 2.5e0
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 25900
  bin: 7.5e0
  variant carriers: 1966
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 13061
  bin: 1.25e1
  variant carriers: 2177
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 2.25e1
  variant carriers: 391
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.25e1
  variant carriers: 150
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 6.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 4.75e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 1.25e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 2.5e0
  variant carriers: 11
num of homozygotes: 217
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-15973633-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973633
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973633
    reference: chr 16
allele count: 1
allele frequency: 1.771793054571226e-5
allele num: 56440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4232A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4232A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+28A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+28A>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4572
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-15973653-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973653
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973653
    reference: chr 16
allele count: 6775
allele frequency: 9.742313997296598e-2
allele num: 69542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4212A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+8A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4212A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+8A>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23908
  bin: 7.5e0
  variant carriers: 620
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 2.5e0
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 1.25e1
  variant carriers: 1796
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.25e1
  variant carriers: 319
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 1.75e1
  variant carriers: 1914
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 2.25e1
  variant carriers: 1111
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 2.75e1
  variant carriers: 548
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 153
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 1.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 22304
  bin: 2.25e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 5.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 2.75e1
  variant carriers: 38
hgvs: c.311+8A>T
num of homozygotes: 375
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

16-15973654-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973654
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973654
    reference: chr 16
allele count: 1
allele frequency: 9.393375791391911e-6
allele num: 106458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4211C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4211C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+7C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+7C>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3841
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
hgvs: c.311+7C>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15973654-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973654
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973654
    reference: chr 16
allele count: 86713
allele frequency: 8.145277949989668e-1
allele num: 106458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4211C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230+7C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4211C>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113+7C>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.5e0
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 14466
  bin: 1.75e1
  variant carriers: 14314
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 523
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 3.25e1
  variant carriers: 2820
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.75e1
  variant carriers: 1889
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 1088
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 1589
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 1.25e1
  variant carriers: 13898
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 7.5e0
  variant carriers: 5035
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.25e1
  variant carriers: 322
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 2.25e1
  variant carriers: 8563
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.25e1
  variant carriers: 764
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 9.75e1
  variant carriers: 1003
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 2.75e1
  variant carriers: 4505
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 160
genotype quality: GenotypeQuality
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 4433
genotype quality: GenotypeQuality
  all individuals: 3902
  bin: 5.25e1
  variant carriers: 3866
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.75e1
  variant carriers: 1474
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 2.5e0
  variant carriers: 194
hgvs: c.311+7C>A
num of homozygotes: 35161
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

16-15973661-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973661
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973661
    reference: chr 16
allele count: 1
allele frequency: 9.245562130177515e-6
allele num: 108160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.383T>C
  hgvsp: ENSP00000461830.1:p.Ile128Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4204T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.383T>C
  hgvsp: ENSP00000461548.1:p.Ile128Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*36T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.311T>C
  hgvsp: ENSP00000255759.6:p.Ile104Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.113T>C
  hgvsp: ENSP00000459429.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.311T>C
  hgvsp: ENSP00000459804.1:p.Ile104Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.230T>C
  hgvsp: ENSP00000458348.1:p.Ile77Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4204T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14925
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile104Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

16-15973670-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973670
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973670
    reference: chr 16
allele count: 1
allele frequency: 9.17094644167278e-6
allele num: 109040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.374A>T
  hgvsp: ENSP00000461830.1:p.Asp125Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.302A>T
  hgvsp: ENSP00000459804.1:p.Asp101Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.302A>T
  hgvsp: ENSP00000255759.6:p.Asp101Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.104A>T
  hgvsp: ENSP00000459429.1:p.Asp35Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.221A>T
  hgvsp: ENSP00000458348.1:p.Asp74Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4195A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4195A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.374A>T
  hgvsp: ENSP00000461548.1:p.Asp125Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*27A>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11092
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp101Val
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: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

16-15973681-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973681
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973681
    reference: chr 16
allele count: 1
allele frequency: 9.033097268391387e-6
allele num: 110704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4184A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.363A>C
  hgvsp: ENSP00000461830.1:p.Glu121Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.93A>C
  hgvsp: ENSP00000459429.1:p.Glu31Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.363A>C
  hgvsp: ENSP00000461548.1:p.Glu121Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4184A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.291A>C
  hgvsp: ENSP00000255759.6:p.Glu97Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.210A>C
  hgvsp: ENSP00000458348.1:p.Glu70Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*16A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.291A>C
  hgvsp: ENSP00000459804.1:p.Glu97Asp
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29169
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu97Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

16-15973687-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973687
    reference: chr 16
allele count: 8
allele frequency: 7.159605505736634e-5
allele num: 111738
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.285A>T
  hgvsp: ENST00000255759.6:c.285A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.285A>T
  hgvsp: ENST00000575073.1:c.285A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*10A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.357A>T
  hgvsp: ENST00000573396.1:c.357A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.204A>T
  hgvsp: ENST00000575938.1:c.204A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4178A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.87A>T
  hgvsp: ENST00000575744.1:c.87A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.357A>T
  hgvsp: ENST00000573429.1:c.357A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4178A>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31636
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala95Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

16-15973695-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973695
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973695
    reference: chr 16
allele count: 1
allele frequency: 8.852377748663291e-6
allele num: 112964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.277C>G
  hgvsp: ENSP00000459804.1:p.Leu93Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.349C>G
  hgvsp: ENSP00000461830.1:p.Leu117Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.277C>G
  hgvsp: ENSP00000255759.6:p.Leu93Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4170C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.196C>G
  hgvsp: ENSP00000458348.1:p.Leu66Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.349C>G
  hgvsp: ENSP00000461548.1:p.Leu117Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.79C>G
  hgvsp: ENSP00000459429.1:p.Leu27Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4170C>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu93Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-15973697-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973697
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973697
    reference: chr 16
allele count: 1
allele frequency: 8.829554284099738e-6
allele num: 113256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.275A>T
  hgvsp: ENSP00000459804.1:p.Glu92Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.77A>T
  hgvsp: ENSP00000459429.1:p.Glu26Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.375A>T
  hgvsp: ENSP00000460592.1:p.Ter125CysextTer5
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.347A>T
  hgvsp: ENSP00000461830.1:p.Glu116Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.275A>T
  hgvsp: ENSP00000255759.6:p.Glu92Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.194A>T
  hgvsp: ENSP00000458348.1:p.Glu65Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.347A>T
  hgvsp: ENSP00000461548.1:p.Glu116Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4168A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4168A>T
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ter125CysextTer5
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS

16-15973703-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973703
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973703
    reference: chr 16
allele count: 1
allele frequency: 8.778860503906592e-6
allele num: 113910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.71T>C
  hgvsp: ENSP00000459429.1:p.Ile24Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.269T>C
  hgvsp: ENSP00000459804.1:p.Ile90Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.369T>C
  hgvsp: ENST00000572415.1:c.369T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.269T>C
  hgvsp: ENSP00000255759.6:p.Ile90Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.188T>C
  hgvsp: ENSP00000458348.1:p.Ile63Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.341T>C
  hgvsp: ENSP00000461548.1:p.Ile114Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4162T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.341T>C
  hgvsp: ENSP00000461830.1:p.Ile114Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4162T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile90Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

16-15973711-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973711
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973711
    reference: chr 16
allele count: 1
allele frequency: 8.744163271016596e-6
allele num: 114362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.361G>A
  hgvsp: ENSP00000460592.1:p.Val121Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.333G>A
  hgvsp: ENST00000573396.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.261G>A
  hgvsp: ENST00000575073.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.261G>A
  hgvsp: ENST00000255759.6:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.180G>A
  hgvsp: ENST00000575938.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4154G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.333G>A
  hgvsp: ENST00000573429.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4154G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.63G>A
  hgvsp: ENST00000575744.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val121Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-15973718-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973718
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973718
    reference: chr 16
allele count: 4
allele frequency: 3.497848822973871e-5
allele num: 114356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4147A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.354A>G
  hgvsp: ENST00000572415.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.56A>G
  hgvsp: ENSP00000459429.1:p.Asp19Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.326A>G
  hgvsp: ENSP00000461830.1:p.Asp109Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.326A>G
  hgvsp: ENSP00000461548.1:p.Asp109Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.254A>G
  hgvsp: ENSP00000255759.6:p.Asp85Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.173A>G
  hgvsp: ENSP00000458348.1:p.Asp58Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.254A>G
  hgvsp: ENSP00000459804.1:p.Asp85Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4147A>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10577
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp85Gly
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

16-15973723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973723
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973723
    reference: chr 16
allele count: 7
allele frequency: 6.138412431162089e-5
allele num: 114036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.249G>A
  hgvsp: ENST00000575073.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4142G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.321G>A
  hgvsp: ENST00000573396.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.321G>A
  hgvsp: ENST00000573429.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.349G>A
  hgvsp: ENSP00000460592.1:p.Val117Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.51G>A
  hgvsp: ENST00000575744.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.249G>A
  hgvsp: ENST00000255759.6:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.168G>A
  hgvsp: ENST00000575938.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4142G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40895
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val117Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

16-15973723-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973723
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973722
    reference: chr 16
allele count: 1
allele frequency: 8.769160615945842e-6
allele num: 114036
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.348delC
  hgvsp: ENSP00000460592.1:p.Val117LeufsTer92
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.320delC
  hgvsp: ENSP00000461548.1:p.Pro107ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.320delC
  hgvsp: ENSP00000461830.1:p.Pro107ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.167delC
  hgvsp: ENSP00000458348.1:p.Pro56ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.248delC
  hgvsp: ENSP00000459804.1:p.Pro83ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4141delC
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.248delC
  hgvsp: ENSP00000255759.6:p.Pro83ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4141delC
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.50delC
  hgvsp: ENSP00000459429.1:p.Pro17ArgfsTer11
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro83ArgfsTer11
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: CG
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

16-15973724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973724
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973724
    reference: chr 16
allele count: 1
allele frequency: 8.791827117511561e-6
allele num: 113742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.348C>T
  hgvsp: ENST00000572415.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.320C>T
  hgvsp: ENSP00000461830.1:p.Pro107Leu
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.50C>T
  hgvsp: ENSP00000459429.1:p.Pro17Leu
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.320C>T
  hgvsp: ENSP00000461548.1:p.Pro107Leu
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4141C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.248C>T
  hgvsp: ENSP00000255759.6:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4141C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.248C>T
  hgvsp: ENSP00000459804.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.167C>T
  hgvsp: ENSP00000458348.1:p.Pro56Leu
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro83Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

16-15973725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973725
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973725
    reference: chr 16
allele count: 10
allele frequency: 8.790281464812503e-5
allele num: 113762
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.247C>T
  hgvsp: ENSP00000255759.6:p.Pro83Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4140C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.319C>T
  hgvsp: ENSP00000461830.1:p.Pro107Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.166C>T
  hgvsp: ENSP00000458348.1:p.Pro56Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.347C>T
  hgvsp: ENSP00000460592.1:p.Ser116Phe
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.49C>T
  hgvsp: ENSP00000459429.1:p.Pro17Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.247C>T
  hgvsp: ENSP00000459804.1:p.Pro83Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4140C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.319C>T
  hgvsp: ENSP00000461548.1:p.Pro107Ser
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33161
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro83Ser
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

16-15973731-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973731
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973731
    reference: chr 16
allele count: 88
allele frequency: 7.828485010230407e-4
allele num: 112410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.160G>A
  hgvsp: ENSP00000458348.1:p.Val54Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4134G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.241G>A
  hgvsp: ENSP00000255759.6:p.Val81Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.341G>A
  hgvsp: ENSP00000460592.1:p.Cys114Tyr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.313G>A
  hgvsp: ENSP00000461830.1:p.Val105Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.313G>A
  hgvsp: ENSP00000461548.1:p.Val105Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.241G>A
  hgvsp: ENSP00000459804.1:p.Val81Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.43G>A
  hgvsp: ENSP00000459429.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4134G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30851
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10990
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3120
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val81Ile
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: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

16-15973748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973748
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973748
    reference: chr 16
allele count: 1
allele frequency: 9.209799226376865e-6
allele num: 108580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4117C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4117C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-3C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3C>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24575
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 9.25e1
  variant carriers: 0
hgvs: c.227-3C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-15973749-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973749
    reference: chr 16
allele count: 3
allele frequency: 2.771977158908211e-5
allele num: 108226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4116C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4116C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-4C>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23993
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
hgvs: c.227-4C>G
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-15973755-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973755
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973755
    reference: chr 16
allele count: 2
allele frequency: 1.877616928594228e-5
allele num: 106518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4110T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-10T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4110T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-10T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

16-15973759-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973759
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973759
    reference: chr 16
allele count: 2
allele frequency: 1.901755320160508e-5
allele num: 105166
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-14T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4106T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4106T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16848
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

16-15973760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973760
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973760
    reference: chr 16
allele count: 1
allele frequency: 9.513842641042717e-6
allele num: 105110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4105A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4105A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-15A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-15A>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16797
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4879
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-15973767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973767
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973767
    reference: chr 16
allele count: 1
allele frequency: 9.728572818367545e-6
allele num: 102790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4098C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4098C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-22C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-22C>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17891
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4878
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16579
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4673
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

16-15973774-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973774
    reference: chr 16
allele count: 7268
allele frequency: 7.264803486465955e-2
allele num: 100044
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4091G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4091G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-29G>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-29G>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 1.75e1
  variant carriers: 1785
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 2.75e1
  variant carriers: 861
genotype depth: GenotypeDepth
  all individuals: 20865
  bin: 1.25e1
  variant carriers: 1256
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 2.25e1
  variant carriers: 1389
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 7.5e0
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 3.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 8.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 3.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 9.25e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 1.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 7.5e0
  variant carriers: 8
num of homozygotes: 379
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-15973782-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973782
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973782
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 94342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4083A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4083A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-37A>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-37A>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15973787-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973787
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973786
    reference: chr 16
allele count: 1
allele frequency: 1.102317070482153e-5
allele num: 90718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4077delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4077delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-43delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-43delT
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5479
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: TA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

16-15973788-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973788
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 90524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4077T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-43T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4077T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21150
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

16-15973794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15973794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15973794
    reference: chr 16
allele count: 1
allele frequency: 1.177662105188779e-5
allele num: 84914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.299-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.227-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.146-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+4071G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.327-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+4071G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.299-49G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.227-49G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14783
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-15976784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976784
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976784
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1081G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1081G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1081G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.298+22G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1081G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.298+22G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.326+22G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3039G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1081G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

16-15976788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976788
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.298+18C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1077C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.326+18C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1077C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.298+18C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1077C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3043C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1077C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1077C>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.5e0
  variant carriers: 24
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-15976796-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976796
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976796
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1069G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1069G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1069G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3051G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1069G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1069G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.326+10G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.298+10G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.298+10G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.5e0
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-15976805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976805
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1060G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1060G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1060G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3060G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.298+1G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.298+1G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.326+1G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1060G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1060G>A
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: splice donor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.5e0
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 7.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
hgvs: c.326+1G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-15976856-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976856
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976856
    reference: chr 16
allele count: 1
allele frequency: 5.0e-1
allele num: 2
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1009T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3111T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.276T>C
  hgvsp: ENST00000572415.1:c.276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1009T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.248T>C
  hgvsp: ENSP00000461830.1:p.Leu83Pro
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.248T>C
  hgvsp: ENSP00000461548.1:p.Leu83Pro
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1009T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1009T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1009T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 2.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 7.5e0
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 2
hgvs: p.Leu83Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-15976908-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976908
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976907
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+956delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3164delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.227-4delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+956delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+956delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+956delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.227-32delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+956delT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.227-32delT
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
hgvs: c.227-4delT
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: CA
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

16-15976925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976925
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976925
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.227-48T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3180T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.227-48T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+940T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+940T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+940T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+940T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+940T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.227-20T>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-15976929-A-AAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976929
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976932
    reference: chr 16
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: AAAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+935_145+936insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+935_226+936insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3185_29-3184insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+935_226+936insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+935_226+936insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.227-53_227-52insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.227-53_227-52insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+935_226+936insCTT
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.227-25_227-24insCTT
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-15976931-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15976931
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15976931
    reference: chr 16
allele count: 1
allele frequency: 5.0e-1
allele num: 2
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+934C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+934C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.227-54C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.227-54C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-3186C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+934C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+934C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+934C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.227-26C>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 2.5e0
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 7.5e0
  variant carriers: 54
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-15977815-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977815
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977815
    reference: chr 16
allele count: 3
allele frequency: 2.926943490477677e-5
allele num: 102496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4070A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+50A>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18720
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14708
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

16-15977826-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977826
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977826
    reference: chr 16
allele count: 9
allele frequency: 8.696828556519722e-5
allele num: 103486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+39C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4081C>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17123
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-15977829-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977829
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977829
    reference: chr 16
allele count: 1
allele frequency: 9.608547764090935e-6
allele num: 104074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4084C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+36C>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3098
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-15977838-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977838
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977838
    reference: chr 16
allele count: 1
allele frequency: 9.379983116030392e-6
allele num: 106610
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4093A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+27A>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9427
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7396
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4308
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31194
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

16-15977846-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977846
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977847
    reference: chr 16
allele count: 2
allele frequency: 1.813006508693366e-5
allele num: 110314
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4102dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+18dupA
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5586
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-15977864-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977864
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977864
    reference: chr 16
allele count: 1
allele frequency: 8.529657619543152e-6
allele num: 117238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.145+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.226+1G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4119G>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.75e1
  variant carriers: 0
hgvs: c.226+1G>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-15977866-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977866
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977866
    reference: chr 16
allele count: 1
allele frequency: 8.492280517010038e-6
allele num: 117754
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.225A>G
  hgvsp: ENST00000255759.6:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.225A>G
  hgvsp: ENST00000572415.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4121A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.225A>G
  hgvsp: ENST00000573087.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.225A>G
  hgvsp: ENST00000575073.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.225A>G
  hgvsp: ENST00000573968.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.225A>G
  hgvsp: ENST00000573429.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.144A>G
  hgvsp: ENST00000575938.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.225A>G
  hgvsp: ENST00000573396.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
hgvs: c.225A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-15977872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977872
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977872
    reference: chr 16
allele count: 4
allele frequency: 3.368591255137102e-5
allele num: 118744
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.219C>T
  hgvsp: ENST00000255759.6:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.219C>T
  hgvsp: ENST00000573396.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.219C>T
  hgvsp: ENST00000573968.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.138C>T
  hgvsp: ENST00000575938.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.219C>T
  hgvsp: ENST00000572415.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4127C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.219C>T
  hgvsp: ENST00000573429.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.219C>T
  hgvsp: ENST00000573087.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.219C>T
  hgvsp: ENST00000575073.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9858
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu73Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-15977877-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977877
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977877
    reference: chr 16
allele count: 9
allele frequency: 7.54881567469637e-5
allele num: 119224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.214G>A
  hgvsp: ENSP00000255759.6:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.214G>A
  hgvsp: ENSP00000460312.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.214G>A
  hgvsp: ENSP00000461548.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.214G>A
  hgvsp: ENSP00000461830.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.214G>A
  hgvsp: ENSP00000458159.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.133G>A
  hgvsp: ENSP00000458348.1:p.Val45Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.214G>A
  hgvsp: ENSP00000460592.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4132G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.214G>A
  hgvsp: ENSP00000459804.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val72Ile
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: C
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

16-15977896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977896
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977896
    reference: chr 16
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.195A>G
  hgvsp: ENST00000575073.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.195A>G
  hgvsp: ENST00000573429.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.195A>G
  hgvsp: ENST00000572415.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.114A>G
  hgvsp: ENST00000575938.1:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.195A>G
  hgvsp: ENST00000573087.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.195A>G
  hgvsp: ENST00000573968.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4151A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.195A>G
  hgvsp: ENST00000255759.6:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.195A>G
  hgvsp: ENST00000573396.1:c.195A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys65Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-15977896-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977896
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977896
    reference: chr 16
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.195A>C
  hgvsp: ENSP00000460312.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.114A>C
  hgvsp: ENSP00000458348.1:p.Lys38Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.195A>C
  hgvsp: ENSP00000255759.6:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.195A>C
  hgvsp: ENSP00000460592.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.195A>C
  hgvsp: ENSP00000458159.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.195A>C
  hgvsp: ENSP00000461548.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.195A>C
  hgvsp: ENSP00000461830.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.195A>C
  hgvsp: ENSP00000459804.1:p.Lys65Asn
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4151A>C
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys65Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-15977901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977901
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977901
    reference: chr 16
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.190A>G
  hgvsp: ENSP00000460312.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4156A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.190A>G
  hgvsp: ENSP00000461830.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.190A>G
  hgvsp: ENSP00000458159.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.190A>G
  hgvsp: ENSP00000460592.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.190A>G
  hgvsp: ENSP00000255759.6:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.190A>G
  hgvsp: ENSP00000459804.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.190A>G
  hgvsp: ENSP00000461548.1:p.Asn64Asp
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.109A>G
  hgvsp: ENSP00000458348.1:p.Asn37Asp
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11201
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn64Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

16-15977907-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977907
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977907
    reference: chr 16
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.184G>A
  hgvsp: ENSP00000255759.6:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.184G>A
  hgvsp: ENSP00000461548.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.184G>A
  hgvsp: ENSP00000460592.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4162G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.103G>A
  hgvsp: ENSP00000458348.1:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.184G>A
  hgvsp: ENSP00000458159.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.184G>A
  hgvsp: ENSP00000461830.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.184G>A
  hgvsp: ENSP00000460312.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.184G>A
  hgvsp: ENSP00000459804.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu62Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

16-15977918-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977918
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977918
    reference: chr 16
allele count: 3
allele frequency: 2.480938125403152e-5
allele num: 120922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.173G>A
  hgvsp: ENSP00000460592.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4173G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.173G>A
  hgvsp: ENSP00000461830.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.173G>A
  hgvsp: ENSP00000458159.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.173G>A
  hgvsp: ENSP00000255759.6:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.92G>A
  hgvsp: ENSP00000458348.1:p.Arg31Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.173G>A
  hgvsp: ENSP00000459804.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.173G>A
  hgvsp: ENSP00000460312.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.173G>A
  hgvsp: ENSP00000461548.1:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg58Gln
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-15977919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977919
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977919
    reference: chr 16
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.172C>T
  hgvsp: ENSP00000458159.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4174C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.172C>T
  hgvsp: ENSP00000460312.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.172C>T
  hgvsp: ENSP00000459804.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.172C>T
  hgvsp: ENSP00000460592.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.91C>T
  hgvsp: ENSP00000458348.1:p.Arg31Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.172C>T
  hgvsp: ENSP00000255759.6:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.172C>T
  hgvsp: ENSP00000461830.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.172C>T
  hgvsp: ENSP00000461548.1:p.Arg58Ter
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48316
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg58Ter
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

16-15977921-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977921
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977921
    reference: chr 16
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.170T>C
  hgvsp: ENSP00000461830.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.170T>C
  hgvsp: ENSP00000255759.6:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.170T>C
  hgvsp: ENSP00000458159.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.170T>C
  hgvsp: ENSP00000460592.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4176T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.170T>C
  hgvsp: ENSP00000459804.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.170T>C
  hgvsp: ENSP00000461548.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.89T>C
  hgvsp: ENSP00000458348.1:p.Ile30Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.170T>C
  hgvsp: ENSP00000460312.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile57Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-15977928-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977928
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977928
    reference: chr 16
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.82G>T
  hgvsp: ENSP00000458348.1:p.Glu28Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.163G>T
  hgvsp: ENSP00000461830.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.163G>T
  hgvsp: ENSP00000461548.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.163G>T
  hgvsp: ENSP00000460312.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.163G>T
  hgvsp: ENSP00000460592.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4183G>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.163G>T
  hgvsp: ENSP00000458159.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.163G>T
  hgvsp: ENSP00000255759.6:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.163G>T
  hgvsp: ENSP00000459804.1:p.Glu55Ter
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu55Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

16-15977937-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977937
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977937
    reference: chr 16
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.154C>G
  hgvsp: ENSP00000460592.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.154C>G
  hgvsp: ENSP00000255759.6:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.154C>G
  hgvsp: ENSP00000458159.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.73C>G
  hgvsp: ENSP00000458348.1:p.Leu25Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4192C>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.154C>G
  hgvsp: ENSP00000459804.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.154C>G
  hgvsp: ENSP00000461548.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.154C>G
  hgvsp: ENSP00000460312.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.154C>G
  hgvsp: ENSP00000461830.1:p.Leu52Val
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu52Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-15977955-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977955
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977954
    reference: chr 16
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.135delA
  hgvsp: ENSP00000461548.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.135delA
  hgvsp: ENSP00000460312.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.135delA
  hgvsp: ENSP00000461830.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.135delA
  hgvsp: ENSP00000458159.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.135delA
  hgvsp: ENSP00000460592.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.135delA
  hgvsp: ENSP00000459804.1:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.135delA
  hgvsp: ENSP00000255759.6:p.Leu46CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.54delA
  hgvsp: ENSP00000458348.1:p.Leu19CysfsTer7
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4211delA
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu46CysfsTer7
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: AT
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

16-15977956-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977956
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977956
    reference: chr 16
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.54A>G
  hgvsp: ENST00000575938.1:c.54A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.135A>G
  hgvsp: ENST00000255759.6:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.135A>G
  hgvsp: ENST00000573396.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.135A>G
  hgvsp: ENST00000573429.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.135A>G
  hgvsp: ENST00000573087.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.135A>G
  hgvsp: ENST00000572415.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.135A>G
  hgvsp: ENST00000573968.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.135A>G
  hgvsp: ENST00000575073.1:c.135A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4211A>G
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser45Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-15977964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977964
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977964
    reference: chr 16
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.127C>T
  hgvsp: ENSP00000458159.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.127C>T
  hgvsp: ENSP00000255759.6:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4219C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.127C>T
  hgvsp: ENSP00000460592.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.127C>T
  hgvsp: ENSP00000461548.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.127C>T
  hgvsp: ENSP00000461830.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.127C>T
  hgvsp: ENSP00000459804.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.127C>T
  hgvsp: ENSP00000460312.1:p.Arg43Ter
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.46C>T
  hgvsp: ENSP00000458348.1:p.Arg16Ter
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg43Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

16-15977972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977972
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977972
    reference: chr 16
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.38G>A
  hgvsp: ENSP00000458348.1:p.Arg13His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.119G>A
  hgvsp: ENSP00000461830.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.119G>A
  hgvsp: ENSP00000459804.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.119G>A
  hgvsp: ENSP00000461548.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.119G>A
  hgvsp: ENSP00000255759.6:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4227G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.119G>A
  hgvsp: ENSP00000460312.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.119G>A
  hgvsp: ENSP00000458159.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.119G>A
  hgvsp: ENSP00000460592.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4748
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg40His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-15977973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977973
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977973
    reference: chr 16
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.118C>T
  hgvsp: ENSP00000460312.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.37C>T
  hgvsp: ENSP00000458348.1:p.Arg13Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.118C>T
  hgvsp: ENSP00000458159.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.118C>T
  hgvsp: ENSP00000461830.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.118C>T
  hgvsp: ENSP00000459804.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.118C>T
  hgvsp: ENSP00000461548.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.118C>T
  hgvsp: ENSP00000255759.6:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.118C>T
  hgvsp: ENSP00000460592.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4228C>T
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  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: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg40Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

16-15977977-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977977
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977977
    reference: chr 16
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.33T>C
  hgvsp: ENST00000575938.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.114T>C
  hgvsp: ENST00000575073.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.114T>C
  hgvsp: ENST00000573396.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.114T>C
  hgvsp: ENST00000573429.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.114T>C
  hgvsp: ENST00000255759.6:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.114T>C
  hgvsp: ENST00000572415.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.114T>C
  hgvsp: ENST00000573087.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4232T>C
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.114T>C
  hgvsp: ENST00000573968.1:c.114T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp38Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-15977978-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977978
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977978
    reference: chr 16
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4233A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.113A>G
  hgvsp: ENSP00000458159.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.32A>G
  hgvsp: ENSP00000458348.1:p.Asp11Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.113A>G
  hgvsp: ENSP00000255759.6:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.113A>G
  hgvsp: ENSP00000459804.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.113A>G
  hgvsp: ENSP00000460312.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.113A>G
  hgvsp: ENSP00000461830.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.113A>G
  hgvsp: ENSP00000461548.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.113A>G
  hgvsp: ENSP00000460592.1:p.Asp38Gly
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp38Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-15977980-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977980
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977979
    reference: chr 16
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.110delA
  hgvsp: ENSP00000460592.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.110delA
  hgvsp: ENSP00000461548.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.110delA
  hgvsp: ENSP00000459804.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.110delA
  hgvsp: ENSP00000255759.6:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4236delA
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.29delA
  hgvsp: ENSP00000458348.1:p.Asp10ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.110delA
  hgvsp: ENSP00000460312.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.110delA
  hgvsp: ENSP00000461830.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.110delA
  hgvsp: ENSP00000458159.1:p.Asp37ValfsTer16
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4749
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp37ValfsTer16
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: AT
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

16-15977983-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977983
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977983
    reference: chr 16
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.108A>G
  hgvsp: ENST00000575073.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.108A>G
  hgvsp: ENST00000573396.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.108A>G
  hgvsp: ENST00000572415.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.108A>G
  hgvsp: ENST00000573429.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.108A>G
  hgvsp: ENST00000573087.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.29-2A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.108A>G
  hgvsp: ENST00000573968.1:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4238A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.108A>G
  hgvsp: ENST00000255759.6:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26435
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41431
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: c.29-2A>G
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

16-15977988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977988
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977988
    reference: chr 16
allele count: 17
allele frequency: 1.400929557965521e-4
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.103G>A
  hgvsp: ENSP00000461548.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.103G>A
  hgvsp: ENSP00000461830.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.103G>A
  hgvsp: ENSP00000255759.6:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.103G>A
  hgvsp: ENSP00000460312.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.29-7G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.103G>A
  hgvsp: ENSP00000458159.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4243G>A
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.103G>A
  hgvsp: ENSP00000459804.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.103G>A
  hgvsp: ENSP00000460592.1:p.Ala35Thr
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala35Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

16-15977990-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15977990
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15977990
    reference: chr 16
allele count: 18
allele frequency: 1.483288285318742e-4
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.29-9A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.101A>G
  hgvsp: ENSP00000460592.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.101A>G
  hgvsp: ENSP00000458159.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.101A>G
  hgvsp: ENSP00000461548.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4245A>G
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.101A>G
  hgvsp: ENSP00000459804.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.101A>G
  hgvsp: ENSP00000461830.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.101A>G
  hgvsp: ENSP00000255759.6:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.101A>G
  hgvsp: ENSP00000460312.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn34Ser
num of homozygotes: 1
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

16-15978002-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15978002
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 15978002
    reference: chr 16
allele count: 11
allele frequency: 9.066482040123304e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000255759
  ensembl transcript: ENST00000255759
  gene symbol: FOPNL
  hgvsc: ENST00000255759.6:c.89C>T
  hgvsp: ENSP00000255759.6:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461548
  ensembl transcript: ENST00000573396
  gene symbol: FOPNL
  hgvsc: ENST00000573396.1:c.89C>T
  hgvsp: ENSP00000461548.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458159
  ensembl transcript: ENST00000573087
  gene symbol: FOPNL
  hgvsc: ENST00000573087.1:c.89C>T
  hgvsp: ENSP00000458159.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459804
  ensembl transcript: ENST00000575073
  gene symbol: FOPNL
  hgvsc: ENST00000575073.1:c.89C>T
  hgvsp: ENSP00000459804.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000458348
  ensembl transcript: ENST00000575938
  gene symbol: FOPNL
  hgvsc: ENST00000575938.1:c.29-21C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460312
  ensembl transcript: ENST00000573968
  gene symbol: FOPNL
  hgvsc: ENST00000573968.1:c.89C>T
  hgvsp: ENSP00000460312.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000461830
  ensembl transcript: ENST00000573429
  gene symbol: FOPNL
  hgvsc: ENST00000573429.1:c.89C>T
  hgvsp: ENSP00000461830.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000459429
  ensembl transcript: ENST00000575744
  gene symbol: FOPNL
  hgvsc: ENST00000575744.1:c.29-4257C>T
  variant of: http://identifiers.org/hgnc/26435
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133393
  ensembl protein: ENSP00000460592
  ensembl transcript: ENST00000572415
  gene symbol: FOPNL
  hgvsc: ENST00000572415.1:c.89C>T
  hgvsp: ENSP00000460592.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/26435
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala30Val
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5848
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21911
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5489
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4531
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 8.27904e5

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.098e1

GenotypeQuality
all individuals: 724
bin: 9.25e1
variant carriers: 259

GenotypeQuality
all individuals: 4035
bin: 2.75e1
variant carriers: 96

GenotypeQuality
all individuals: 4955
bin: 7.5e0
variant carriers: 47

GenotypeQuality
all individuals: 3887
bin: 6.25e1
variant carriers: 126

GenotypeQuality
all individuals: 19974
bin: 2.25e1
variant carriers: 175

GenotypeQuality
all individuals: 2593
bin: 3.75e1
variant carriers: 73

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 133

GenotypeQuality
all individuals: 396
bin: 5.25e1
variant carriers: 127

GenotypeQuality
all individuals: 560
bin: 7.25e1
variant carriers: 34

GenotypeQuality
all individuals: 4826
bin: 3.25e1
variant carriers: 81

GenotypeQuality
all individuals: 513
bin: 8.75e1
variant carriers: 184

GenotypeQuality
all individuals: 887
bin: 7.75e1
variant carriers: 78

GenotypeQuality
all individuals: 7511
bin: 9.75e1
variant carriers: 4494

GenotypeQuality
all individuals: 710
bin: 4.25e1
variant carriers: 56

GenotypeQuality
all individuals: 776
bin: 8.25e1
variant carriers: 133

East Asian
type: Population
allele count: 986
allele frequency: 2.696936542669584e-1
allele num: 3656
num of homozygotes: 107

South Asian
type: Population
allele count: 392
allele frequency: 3.852958521722036e-2
allele num: 10174
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 1924
allele frequency: 6.966975666280417e-2
allele num: 27616
num of homozygotes: 55

European (Finnish)
type: Population
allele count: 138
allele frequency: 3.436254980079681e-2
allele num: 4016
num of homozygotes: 3

Latino
type: Population
allele count: 465
allele frequency: 1.276070252469813e-1
allele num: 3644
num of homozygotes: 20

Other
type: Population
allele count: 33
allele frequency: 6.547619047619048e-2
allele num: 504
num of homozygotes: 1

African
type: Population
allele count: 548
allele frequency: 9.644491376275958e-2
allele num: 5682
num of homozygotes: 19

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-1

FS
type: SiteQuality
SIO_000300: 4.512e0

DP
type: SiteQuality
SIO_000300: 8.54131e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.72e-2

MQ
type: SiteQuality
SIO_000300: 5.845e1

QD
type: SiteQuality
SIO_000300: 1.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 4851
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23074
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5687
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3846
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.652519893899204e-4
allele num: 3770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4056
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 8.71904e5

VQSLOD
type: SiteQuality
SIO_000300: -1.85e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.038e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 108

GenotypeQuality
all individuals: 669
bin: 4.75e1
variant carriers: 71

GenotypeQuality
all individuals: 9337
bin: 6.25e1
variant carriers: 59

GenotypeQuality
all individuals: 1649
bin: 6.75e1
variant carriers: 58

GenotypeQuality
all individuals: 8974
bin: 9.75e1
variant carriers: 5942

GenotypeQuality
all individuals: 1655
bin: 3.75e1
variant carriers: 66

GenotypeQuality
all individuals: 1099
bin: 7.75e1
variant carriers: 104

GenotypeQuality
all individuals: 3520
bin: 3.25e1
variant carriers: 55

GenotypeQuality
all individuals: 483
bin: 1.25e1
variant carriers: 32

GenotypeQuality
all individuals: 443
bin: 4.25e1
variant carriers: 37

GenotypeQuality
all individuals: 580
bin: 9.25e1
variant carriers: 91

GenotypeQuality
all individuals: 426
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 708
bin: 7.25e1
variant carriers: 59

GenotypeQuality
all individuals: 1396
bin: 7.5e0
variant carriers: 27

GenotypeQuality
all individuals: 970
bin: 5.25e1
variant carriers: 59

GenotypeQuality
all individuals: 864
bin: 8.25e1
variant carriers: 107

Latino
type: Population
allele count: 784
allele frequency: 1.475903614457831e-1
allele num: 5312
num of homozygotes: 36

European (Non-Finnish)
type: Population
allele count: 2917
allele frequency: 8.214587440157702e-2
allele num: 35510
num of homozygotes: 97

South Asian
type: Population
allele count: 502
allele frequency: 4.4974018993012e-2
allele num: 11162
num of homozygotes: 14

Other
type: Population
allele count: 44
allele frequency: 7.333333333333333e-2
allele num: 600
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 164
allele frequency: 3.54824751189961e-2
allele num: 4622
num of homozygotes: 3

East Asian
type: Population
allele count: 1623
allele frequency: 2.974706744868035e-1
allele num: 5456
num of homozygotes: 189

African
type: Population
allele count: 741
allele frequency: 1.07703488372093e-1
allele num: 6880
num of homozygotes: 35

DP
type: SiteQuality
SIO_000300: 1.038158e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.13e-2

QD
type: SiteQuality
SIO_000300: 1.538e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

MQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 1.627e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e-1

GenotypeQuality
all individuals: 4422
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.072271070126528e-4
allele num: 9326
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

QD
type: SiteQuality
SIO_000300: 2.773e1

FS
type: SiteQuality
SIO_000300: 2.353e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.40117e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

GenotypeQuality
all individuals: 1202
bin: 8.25e1
variant carriers: 1159

GenotypeQuality
all individuals: 1094
bin: 1.75e1
variant carriers: 1068

GenotypeQuality
all individuals: 1625
bin: 2.75e1
variant carriers: 1490

GenotypeQuality
all individuals: 2389
bin: 4.25e1
variant carriers: 2353

GenotypeQuality
all individuals: 2589
bin: 2.25e1
variant carriers: 1981

GenotypeQuality
all individuals: 667
bin: 8.75e1
variant carriers: 627

GenotypeQuality
all individuals: 982
bin: 9.25e1
variant carriers: 944

GenotypeQuality
all individuals: 389
bin: 7.5e0
variant carriers: 345

GenotypeQuality
all individuals: 3841
bin: 3.25e1
variant carriers: 3714

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 2105

GenotypeQuality
all individuals: 426
bin: 1.25e1
variant carriers: 400

GenotypeQuality
all individuals: 1722
bin: 5.75e1
variant carriers: 1699

GenotypeQuality
all individuals: 21966
bin: 9.75e1
variant carriers: 21712

GenotypeQuality
all individuals: 912
bin: 7.25e1
variant carriers: 879

GenotypeQuality
all individuals: 3421
bin: 6.25e1
variant carriers: 2782

GenotypeQuality
all individuals: 4422
bin: 4.75e1
variant carriers: 4392

South Asian
type: Population
allele count: 10517
allele frequency: 7.190619444824285e-1
allele num: 14626
num of homozygotes: 3764

East Asian
type: Population
allele count: 5680
allele frequency: 7.567279509725553e-1
allele num: 7506
num of homozygotes: 2088

European (Non-Finnish)
type: Population
allele count: 48013
allele frequency: 8.311924381968008e-1
allele num: 57764
num of homozygotes: 19811

Other
type: Population
allele count: 670
allele frequency: 8.111380145278451e-1
allele num: 826
num of homozygotes: 274

European (Finnish)
type: Population
allele count: 5422
allele frequency: 8.717041800643087e-1
allele num: 6220
num of homozygotes: 2361

African
type: Population
allele count: 7431
allele frequency: 7.968046322110229e-1
allele num: 9326
num of homozygotes: 2938

Latino
type: Population
allele count: 8980
allele frequency: 8.812561334641805e-1
allele num: 10190
num of homozygotes: 3925

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

FS
type: SiteQuality
SIO_000300: 2.353e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.57e-2

DP
type: SiteQuality
SIO_000300: 1.40117e6

QD
type: SiteQuality
SIO_000300: 2.773e1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

GenotypeQuality
all individuals: 4865
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6645
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5662
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18313
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.282380097460887e-4
allele num: 7798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14696
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.319358e6

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.141e0

FS
type: SiteQuality
SIO_000300: 1.335e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeQuality
all individuals: 4866
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6788
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25701
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.688960951222808e-5
allele num: 59208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.376026e6

QD
type: SiteQuality
SIO_000300: 1.319e1

GenotypeQuality
all individuals: 569
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6117
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.661571181709424e-5
allele num: 60184
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.94e0

QD
type: SiteQuality
SIO_000300: 7.52e0

FS
type: SiteQuality
SIO_000300: 3.882e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.450704e6

VQSLOD
type: SiteQuality
SIO_000300: -3.198e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 1977
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4883
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.869508319312021e-4
allele num: 10698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.874917709019091e-5
allele num: 60760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15164
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

FS
type: SiteQuality
SIO_000300: 1.0072e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

DP
type: SiteQuality
SIO_000300: 1.480364e6

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
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GenotypeQuality
all individuals: 906
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 660
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626227801990503e-5
allele num: 61492
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.510137e6

VQSLOD
type: SiteQuality
SIO_000300: 3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.02e-1

QD
type: SiteQuality
SIO_000300: 1.794e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
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variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.018537380321858e-4
allele num: 9818
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.515187e6

VQSLOD
type: SiteQuality
SIO_000300: -1.124e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.812e1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

FS
type: SiteQuality
SIO_000300: 2.332e0

GenotypeQuality
all individuals: 931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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: 2.25e1
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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 663
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.203369434416366e-4
allele num: 8310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10918
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.855e1

FS
type: SiteQuality
SIO_000300: 1.637e0

VQSLOD
type: SiteQuality
SIO_000300: -2.185e0

DP
type: SiteQuality
SIO_000300: 1.530183e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 8.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

QD
type: SiteQuality
SIO_000300: 1.709e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
all individuals: 324
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
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GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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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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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62328
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.200768491834774e-4
allele num: 8328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.845e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 4.052e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 1.540673e6

QD
type: SiteQuality
SIO_000300: 7.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.469e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

GenotypeQuality
all individuals: 4889
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
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GenotypeQuality
all individuals: 4589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
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GenotypeQuality
all individuals: 3256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.75e1
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GenotypeQuality
all individuals: 1162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.417043667982161e-5
allele num: 62334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.542195e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 9.399999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.41e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 577
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 915
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4889
bin: 9.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.157407407407407e-3
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.436663233779608e-5
allele num: 62144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.399808015358771e-4
allele num: 8334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 8.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

DP
type: SiteQuality
SIO_000300: 1.539072e6

GenotypeQuality
all individuals: 565
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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GenotypeQuality
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GenotypeQuality
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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: 224
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GenotypeQuality
all individuals: 4889
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 9.139097057210747e-5
allele num: 10942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.539072e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

FS
type: SiteQuality
SIO_000300: 4.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

QD
type: SiteQuality
SIO_000300: 8.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
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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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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
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 4884
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.202790473899447e-4
allele num: 8314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15396
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -2.351e0

DP
type: SiteQuality
SIO_000300: 1.535351e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 3.726e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

QD
type: SiteQuality
SIO_000300: 2.497e1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

GenotypeQuality
all individuals: 3221
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4885
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
all individuals: 588
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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
all individuals: 908
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5274
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.491820306413919e-4
allele num: 15404
num of homozygotes: 1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.206e1

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

FS
type: SiteQuality
SIO_000300: 5.094e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.525e0

DP
type: SiteQuality
SIO_000300: 1.535966e6

VQSLOD
type: SiteQuality
SIO_000300: 9.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.49e-2

GenotypeQuality
all individuals: 441
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
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variant carriers: 0

GenotypeQuality
all individuals: 4962
bin: 9.75e1
variant carriers: 87

GenotypeQuality
all individuals: 31
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GenotypeQuality
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bin: 6.25e1
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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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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: 431
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variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 87
allele frequency: 1.42314990512334e-3
allele num: 61132
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027749229188078e-4
allele num: 9730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.581e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

DP
type: SiteQuality
SIO_000300: 1.514443e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.071e1

GenotypeQuality
all individuals: 225
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
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GenotypeQuality
all individuals: 4880
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
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GenotypeQuality
all individuals: 31478
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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: 0

GenotypeQuality
all individuals: 766
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
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: 0
allele frequency: 0.0e0
allele num: 14810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58784
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.05999576001696e-4
allele num: 9434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8040
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.063e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.434647e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.689e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 1952
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GenotypeQuality
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GenotypeQuality
all individuals: 240
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GenotypeQuality
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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: 662
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GenotypeQuality
all individuals: 350
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.120152921900601e-5
allele num: 58592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 3.924e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.235e0

VQSLOD
type: SiteQuality
SIO_000300: 9.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.357e0

DP
type: SiteQuality
SIO_000300: 1.427054e6

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 14233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
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GenotypeQuality
all individuals: 660
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GenotypeQuality
all individuals: 393
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1008
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variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
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GenotypeQuality
all individuals: 2693
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
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GenotypeQuality
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GenotypeQuality
all individuals: 4879
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1336
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57584
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.149613069647464e-4
allele num: 9304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

DP
type: SiteQuality
SIO_000300: 1.377426e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

GenotypeQuality
all individuals: 2979
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1795
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.762114537444934e-5
allele num: 56750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -2.168e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 1.5527e1

DP
type: SiteQuality
SIO_000300: 1.333618e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.525e1

GenotypeQuality
all individuals: 424
bin: 8.75e1
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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GenotypeQuality
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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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.763108713283261e-5
allele num: 56718
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.617e1

VQSLOD
type: SiteQuality
SIO_000300: -2.622e0

DP
type: SiteQuality
SIO_000300: 1.333599e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.702e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 9.05e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

GenotypeQuality
all individuals: 856
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 850
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GenotypeQuality
all individuals: 967
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.80766449746927e-5
allele num: 55320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14230
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.818e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.95e-1

FS
type: SiteQuality
SIO_000300: 5.229e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

QD
type: SiteQuality
SIO_000300: 1.465e1

DP
type: SiteQuality
SIO_000300: 1.26686e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

VQSLOD
type: SiteQuality
SIO_000300: -2.764e-1

GenotypeQuality
all individuals: 5356
bin: 3.25e1
variant carriers: 24

GenotypeQuality
all individuals: 18893
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variant carriers: 22

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 52

GenotypeQuality
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variant carriers: 15

GenotypeQuality
all individuals: 252
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variant carriers: 52

GenotypeQuality
all individuals: 1493
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variant carriers: 60

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
all individuals: 9670
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variant carriers: 62

GenotypeQuality
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variant carriers: 31

GenotypeQuality
all individuals: 291
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variant carriers: 64

GenotypeQuality
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variant carriers: 38

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 69

GenotypeQuality
all individuals: 10848
bin: 9.75e1
variant carriers: 6502

African
type: Population
allele count: 790
allele frequency: 8.969118982742962e-2
allele num: 8808
num of homozygotes: 36

European (Finnish)
type: Population
allele count: 173
allele frequency: 2.883333333333333e-2
allele num: 6000
num of homozygotes: 3

Other
type: Population
allele count: 48
allele frequency: 6.075949367088607e-2
allele num: 790
num of homozygotes: 1

South Asian
type: Population
allele count: 549
allele frequency: 3.917511060368203e-2
allele num: 14014
num of homozygotes: 17

European (Non-Finnish)
type: Population
allele count: 3129
allele frequency: 5.826598636922275e-2
allele num: 53702
num of homozygotes: 92

Latino
type: Population
allele count: 815
allele frequency: 8.782327586206896e-2
allele num: 9280
num of homozygotes: 29

East Asian
type: Population
allele count: 1764
allele frequency: 2.367785234899329e-1
allele num: 7450
num of homozygotes: 201

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

DP
type: SiteQuality
SIO_000300: 1.228343e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.48e-2

FS
type: SiteQuality
SIO_000300: 7.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.58e-1

QD
type: SiteQuality
SIO_000300: 1.546e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

GenotypeQuality
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bin: 4.75e1
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
all individuals: 533
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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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GenotypeQuality
all individuals: 1200
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variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 631
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.308e1

DP
type: SiteQuality
SIO_000300: 1.111676e6

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

FS
type: SiteQuality
SIO_000300: 4.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 520
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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
all individuals: 391
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4590
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.072710691041744e-5
allele num: 48246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8068
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

DP
type: SiteQuality
SIO_000300: 1.083028e6

FS
type: SiteQuality
SIO_000300: 1.264e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.135e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.907e1

GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18412
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5766
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48120
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.38e-1

MQ
type: SiteQuality
SIO_000300: 5.652e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

DP
type: SiteQuality
SIO_000300: 1.078851e6

QD
type: SiteQuality
SIO_000300: 2.488e1

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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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2171
bin: 4.75e1
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GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.229753835176596e-5
allele num: 44848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.062369e6

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.031e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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African
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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VQSLOD
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MQRankSum
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QD
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DP
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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MQ
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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Other
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African
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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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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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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MQ
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FS
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VQSLOD
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QD
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DP
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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DP
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FS
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.338688085676038e-4
allele num: 7470
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.804402742692169e-5
allele num: 55420
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.471607890017931e-5
allele num: 13384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

DP
type: SiteQuality
SIO_000300: 1.059964e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13616
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.608924166040974e-4
allele num: 55938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.416e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

BaseQRankSum
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.124128e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56298
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13712
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.325556733828208e-4
allele num: 7544
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

FS
type: SiteQuality
SIO_000300: 9.717000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

VQSLOD
type: SiteQuality
SIO_000300: -1.759e0

DP
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SIO_000300: 1.151537e6

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.734725739860528e-5
allele num: 57646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.771e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.239e0

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

BaseQRankSum
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SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

DP
type: SiteQuality
SIO_000300: 1.249193e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-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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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: 10032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

Latino
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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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.343810606567244e-5
allele num: 59812
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.330919e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.560939060939061e-5
allele num: 64064
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.064e1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8454
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.969e1

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.153656810559675e-5
allele num: 65002
num of homozygotes: 0

Latino
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Other
type: Population
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South Asian
type: Population
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allele frequency: 0.0e0
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African
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East Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
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: 9
allele frequency: 1.055347091932458e-3
allele num: 8528
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.461964e6

FS
type: SiteQuality
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QD
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ClippingRankSum
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SIO_000300: 1.37e-1

InbreedingCoeff
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SIO_000300: 5.7e-3

BaseQRankSum
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SIO_000300: -2.783e0

MQRankSum
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SIO_000300: 6.64e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.404e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66060
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

South Asian
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allele frequency: 6.110975311659741e-5
allele num: 16364
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8586
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FS
type: SiteQuality
SIO_000300: 9.631e0

ReadPosRankSum
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SIO_000300: 2.34e-1

MQRankSum
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DP
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.951e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.93e-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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
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East Asian
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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: 904
num of homozygotes: 0

Latino
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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: 1.513775355737209e-5
allele num: 66060
num of homozygotes: 0

South Asian
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FS
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SIO_000300: 9.631e0

ReadPosRankSum
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SIO_000300: 2.34e-1

VQSLOD
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InbreedingCoeff
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DP
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MQ
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 5.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.93e-1

QD
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SIO_000300: 1.546e1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66166
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 6.956e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.099048548426445e-5
allele num: 16396
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.809e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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SIO_000300: 4.96e-1

FS
type: SiteQuality
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ReadPosRankSum
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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GenotypeQuality
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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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num of homozygotes: 0

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

Latino
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: 2
allele frequency: 3.008876184744998e-5
allele num: 66470
num of homozygotes: 0

East Asian
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allele num: 8624
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele num: 16430
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

Other
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQ
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Latino
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European (Finnish)
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South Asian
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MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66566
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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DP
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.000930288389401e-5
allele num: 66646
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South Asian
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African
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MQ
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QD
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MQRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11562
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European (Non-Finnish)
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allele frequency: 1.498890820792613e-5
allele num: 66716
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BaseQRankSum
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DP
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MQRankSum
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MQ
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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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

East Asian
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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: 6612
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Other
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African
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allele frequency: 0.0e0
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South Asian
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Latino
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

VQSLOD
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SIO_000300: 3.12e0

ClippingRankSum
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SIO_000300: -8.3e-2

FS
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

South Asian
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allele num: 16496
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66720
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Latino
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Other
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East Asian
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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Latino
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 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: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 1.459e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

DP
type: SiteQuality
SIO_000300: 1.497609e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 16506
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 count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
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East Asian
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VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
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SIO_000300: 1.497667e6

MQ
type: SiteQuality
SIO_000300: 6.02e1

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.343e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
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BaseQRankSum
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SIO_000300: 3.22e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.497635e6

InbreedingCoeff
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SIO_000300: 0.0e0

QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele num: 11564
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South Asian
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 16
allele frequency: 2.397722163944253e-4
allele num: 66730
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
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FS
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SIO_000300: 3.251e0

DP
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SIO_000300: 1.498548e6

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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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: 17

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

African
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allele frequency: 0.0e0
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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 frequency: 2.997062878379188e-5
allele num: 66732
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Other
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South Asian
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allele count: 16
allele frequency: 9.69227041434456e-4
allele num: 16508
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 1.73e0

DP
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QD
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BaseQRankSum
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SIO_000300: 2.61e0