16-419088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419088
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419088
    reference: chr 16
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.439C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.421C>T
  hgvsp: ENSP00000390399.1:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.421C>T
  hgvsp: ENSP00000395305.1:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.419C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.421C>T
  hgvsp: ENSP00000374326.2:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1166C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.421C>T
  hgvsp: ENSP00000398684.1:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.437C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.421C>T
  hgvsp: ENSP00000199706.7:p.Leu141Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+506C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu141Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-419089-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419089
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419089
    reference: chr 16
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.436G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.420G>T
  hgvsp: ENST00000199706.8:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.420G>T
  hgvsp: ENST00000450882.1:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1165G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.418G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.420G>T
  hgvsp: ENST00000389675.2:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.420G>T
  hgvsp: ENST00000447696.1:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.420G>T
  hgvsp: ENST00000441883.1:c.420G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+505G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.438G>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly140Gly
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-419091-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419091
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419091
    reference: chr 16
allele count: 8
allele frequency: 6.61802418887841e-5
allele num: 120882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.418G>A
  hgvsp: ENSP00000395305.1:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1163G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.418G>A
  hgvsp: ENSP00000398684.1:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.434G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.436G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+503G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.418G>A
  hgvsp: ENSP00000390399.1:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.418G>A
  hgvsp: ENSP00000374326.2:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.418G>A
  hgvsp: ENSP00000199706.7:p.Gly140Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.416G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly140Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

16-419092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419092
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419092
    reference: chr 16
allele count: 74671
allele frequency: 6.166162942410279e-1
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.415T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.417T>C
  hgvsp: ENST00000389675.2:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.417T>C
  hgvsp: ENST00000441883.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.435T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.433T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.417T>C
  hgvsp: ENST00000199706.8:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.417T>C
  hgvsp: ENST00000450882.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1162T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.417T>C
  hgvsp: ENST00000447696.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+502T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.75e1
  variant carriers: 1467
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.25e1
  variant carriers: 3468
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 2.25e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 5.25e1
  variant carriers: 5415
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 3.25e1
  variant carriers: 1429
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 2.75e1
  variant carriers: 702
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 8.25e1
  variant carriers: 2051
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 9.75e1
  variant carriers: 5183
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 4.75e1
  variant carriers: 4692
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 6.75e1
  variant carriers: 4655
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 5.75e1
  variant carriers: 5829
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 7.75e1
  variant carriers: 2850
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.75e1
  variant carriers: 2403
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 7.25e1
  variant carriers: 3761
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.25e1
  variant carriers: 1035
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 6.25e1
  variant carriers: 5479
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 8.25e1
  variant carriers: 228
hgvs: p.Tyr139Tyr
num of homozygotes: 23740
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-419094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419094
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419094
    reference: chr 16
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.431T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.415T>C
  hgvsp: ENSP00000395305.1:p.Tyr139His
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.415T>C
  hgvsp: ENSP00000390399.1:p.Tyr139His
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.415T>C
  hgvsp: ENSP00000398684.1:p.Tyr139His
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.415T>C
  hgvsp: ENSP00000374326.2:p.Tyr139His
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+500T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.413T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1160T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.415T>C
  hgvsp: ENSP00000199706.7:p.Tyr139His
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.433T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5665
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr139His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

16-419098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419098
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419098
    reference: chr 16
allele count: 5
allele frequency: 4.125140254768662e-5
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.409G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.411G>A
  hgvsp: ENST00000447696.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.427G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.411G>A
  hgvsp: ENST00000450882.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.411G>A
  hgvsp: ENST00000389675.2:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.429G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+496G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.411G>A
  hgvsp: ENST00000441883.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.411G>A
  hgvsp: ENST00000199706.8:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1156G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28279
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu137Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

16-419101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419101
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419101
    reference: chr 16
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.424T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.408T>C
  hgvsp: ENST00000389675.2:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.426T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1153T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.408T>C
  hgvsp: ENST00000450882.1:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.408T>C
  hgvsp: ENST00000441883.1:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+493T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.408T>C
  hgvsp: ENST00000447696.1:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.408T>C
  hgvsp: ENST00000199706.8:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.406T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28321
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp136Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

16-419103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419103
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419103
    reference: chr 16
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.424G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.406G>A
  hgvsp: ENSP00000390399.1:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.406G>A
  hgvsp: ENSP00000199706.7:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.406G>A
  hgvsp: ENSP00000374326.2:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.404G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.406G>A
  hgvsp: ENSP00000395305.1:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.422G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1151G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.406G>A
  hgvsp: ENSP00000398684.1:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+491G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp136Asn
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

16-419104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419104
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419104
    reference: chr 16
allele count: 4
allele frequency: 3.299731071917638e-5
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.405C>T
  hgvsp: ENST00000389675.2:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.423C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.405C>T
  hgvsp: ENST00000447696.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.405C>T
  hgvsp: ENST00000199706.8:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.403C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.405C>T
  hgvsp: ENST00000450882.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+490C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.405C>T
  hgvsp: ENST00000441883.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1150C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.421C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile135Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

16-419109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419109
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419109
    reference: chr 16
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.416C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.400C>T
  hgvsp: ENSP00000390399.1:p.Leu134Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.400C>T
  hgvsp: ENSP00000395305.1:p.Leu134Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.418C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1145C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.400C>T
  hgvsp: ENSP00000374326.2:p.Leu134Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.398C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.400C>T
  hgvsp: ENSP00000398684.1:p.Leu134Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.400C>T
  hgvsp: ENSP00000199706.7:p.Leu134Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+485C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu134Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-419112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419112
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419112
    reference: chr 16
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.395G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.397G>A
  hgvsp: ENSP00000398684.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.397G>A
  hgvsp: ENSP00000395305.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1142G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.397G>A
  hgvsp: ENSP00000374326.2:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+482G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.397G>A
  hgvsp: ENSP00000199706.7:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.397G>A
  hgvsp: ENSP00000390399.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.413G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.415G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp133Asn
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

16-419113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419113
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419113
    reference: chr 16
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.412G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+481G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.396G>A
  hgvsp: ENST00000447696.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.396G>A
  hgvsp: ENST00000389675.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.396G>A
  hgvsp: ENST00000199706.8:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.396G>A
  hgvsp: ENST00000441883.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1141G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.396G>A
  hgvsp: ENST00000450882.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.414G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.394G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu132Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

16-419114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419114
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419114
    reference: chr 16
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1140T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.395T>C
  hgvsp: ENSP00000199706.7:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.411T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.395T>C
  hgvsp: ENSP00000374326.2:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.395T>C
  hgvsp: ENSP00000390399.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.393T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+480T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.395T>C
  hgvsp: ENSP00000398684.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.395T>C
  hgvsp: ENSP00000395305.1:p.Leu132Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.413T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu132Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

16-419120-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419120
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419120
    reference: chr 16
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.407G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.389G>C
  hgvsp: ENSP00000199706.7:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.389G>C
  hgvsp: ENSP00000374326.2:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.405G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.389G>C
  hgvsp: ENSP00000390399.1:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.389G>C
  hgvsp: ENSP00000395305.1:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.389G>C
  hgvsp: ENSP00000398684.1:p.Arg130Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.387G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+474G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1134G>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg130Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-419120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419120
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419120
    reference: chr 16
allele count: 11
allele frequency: 9.073062901070621e-5
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1134G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.389G>A
  hgvsp: ENSP00000374326.2:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.389G>A
  hgvsp: ENSP00000390399.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.389G>A
  hgvsp: ENSP00000199706.7:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.407G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.389G>A
  hgvsp: ENSP00000395305.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.387G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.389G>A
  hgvsp: ENSP00000398684.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.405G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+474G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg130Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-419121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419121
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419121
    reference: chr 16
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.388C>T
  hgvsp: ENSP00000395305.1:p.Arg130Trp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.388C>T
  hgvsp: ENSP00000390399.1:p.Arg130Trp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+473C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.406C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.386C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.388C>T
  hgvsp: ENSP00000199706.7:p.Arg130Trp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1133C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.404C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.388C>T
  hgvsp: ENSP00000374326.2:p.Arg130Trp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.388C>T
  hgvsp: ENSP00000398684.1:p.Arg130Trp
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg130Trp
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

16-419126-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419126
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419126
    reference: chr 16
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.401C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.399C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.383C>G
  hgvsp: ENSP00000374326.2:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1128C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.383C>G
  hgvsp: ENSP00000199706.7:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.383C>G
  hgvsp: ENSP00000390399.1:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.381C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.383C>G
  hgvsp: ENSP00000398684.1:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.383C>G
  hgvsp: ENSP00000395305.1:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+468C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr128Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-419128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419128
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419128
    reference: chr 16
allele count: 6
allele frequency: 4.948698492296526e-5
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.381G>A
  hgvsp: ENST00000447696.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.379G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.381G>A
  hgvsp: ENST00000441883.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.397G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.399G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.381G>A
  hgvsp: ENST00000389675.2:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.381G>A
  hgvsp: ENST00000450882.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.381G>A
  hgvsp: ENST00000199706.8:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1126G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+466G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val127Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

16-419133-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419133
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419133
    reference: chr 16
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.376A>C
  hgvsp: ENSP00000390399.1:p.Thr126Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.376A>C
  hgvsp: ENSP00000395305.1:p.Thr126Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.392A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+461A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.376A>C
  hgvsp: ENSP00000199706.7:p.Thr126Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.376A>C
  hgvsp: ENSP00000374326.2:p.Thr126Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.376A>C
  hgvsp: ENSP00000398684.1:p.Thr126Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1121A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.374A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.394A>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr126Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-419137-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419137
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419137
    reference: chr 16
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.390A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.372A>T
  hgvsp: ENST00000389675.2:c.372A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1117A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.372A>T
  hgvsp: ENST00000447696.1:c.372A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.372A>T
  hgvsp: ENST00000441883.1:c.372A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.372A>T
  hgvsp: ENST00000450882.1:c.372A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.370A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+457A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.372A>T
  hgvsp: ENST00000199706.8:c.372A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.388A>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr124Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-419137-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419137
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419137
    reference: chr 16
allele count: 3
allele frequency: 2.474104374216534e-5
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.372A>G
  hgvsp: ENST00000447696.1:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.372A>G
  hgvsp: ENST00000450882.1:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.388A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.372A>G
  hgvsp: ENST00000389675.2:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.372A>G
  hgvsp: ENST00000199706.8:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.372A>G
  hgvsp: ENST00000441883.1:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1117A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.370A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.390A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+457A>G
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28543
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr124Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-419151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419151
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419151
    reference: chr 16
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.376G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.358G>A
  hgvsp: ENSP00000398684.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.358G>A
  hgvsp: ENSP00000395305.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.358G>A
  hgvsp: ENSP00000390399.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.374G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.358G>A
  hgvsp: ENSP00000199706.7:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.358G>A
  hgvsp: ENSP00000374326.2:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1103G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.356G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+443G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28580
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp120Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-419152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419152
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419152
    reference: chr 16
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.375G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.357G>A
  hgvsp: ENST00000199706.8:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+442G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.357G>A
  hgvsp: ENST00000441883.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.357G>A
  hgvsp: ENST00000450882.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.357G>A
  hgvsp: ENST00000389675.2:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.357G>A
  hgvsp: ENST00000447696.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.355G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1102G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.373G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu119Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

16-419154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419154
    reference: chr 16
allele count: 16706
allele frequency: 1.37767808546783e-1
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.355C>T
  hgvsp: ENST00000199706.8:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+440C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.355C>T
  hgvsp: ENST00000389675.2:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.353C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1100C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.355C>T
  hgvsp: ENST00000450882.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.371C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.355C>T
  hgvsp: ENST00000447696.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.355C>T
  hgvsp: ENST00000441883.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.373C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 5.25e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 5.75e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 4.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 6.75e1
  variant carriers: 812
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.25e1
  variant carriers: 1105
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.25e1
  variant carriers: 978
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 9.75e1
  variant carriers: 6691
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 3.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 6.25e1
  variant carriers: 685
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 4.75e1
  variant carriers: 291
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 8.25e1
  variant carriers: 1206
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 1208
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 7.75e1
  variant carriers: 1113
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu119Leu
num of homozygotes: 1306
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-419158-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419158
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419158
    reference: chr 16
allele count: 3
allele frequency: 2.473655568198684e-5
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.351G>C
  hgvsp: ENSP00000398684.1:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.351G>C
  hgvsp: ENSP00000199706.7:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.349G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.351G>C
  hgvsp: ENSP00000374326.2:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+436G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.367G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1096G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.351G>C
  hgvsp: ENSP00000395305.1:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.369G>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.351G>C
  hgvsp: ENSP00000390399.1:p.Glu117Asp
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu117Asp
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: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-419166-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419166
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419166
    reference: chr 16
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.343T>A
  hgvsp: ENSP00000199706.7:p.Tyr115Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.343T>A
  hgvsp: ENSP00000395305.1:p.Tyr115Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.343T>A
  hgvsp: ENSP00000398684.1:p.Tyr115Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.343T>A
  hgvsp: ENSP00000374326.2:p.Tyr115Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.361T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.359T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1088T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.343T>A
  hgvsp: ENSP00000390399.1:p.Tyr115Asn
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+428T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.341T>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr115Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-419168-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419168
    reference: chr 16
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.341T>C
  hgvsp: ENSP00000199706.7:p.Phe114Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.341T>C
  hgvsp: ENSP00000398684.1:p.Phe114Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.341T>C
  hgvsp: ENSP00000390399.1:p.Phe114Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.339T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+426T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.359T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.341T>C
  hgvsp: ENSP00000395305.1:p.Phe114Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.357T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.341T>C
  hgvsp: ENSP00000374326.2:p.Phe114Ser
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1086T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe114Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ

16-419170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419170
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419170
    reference: chr 16
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.339G>A
  hgvsp: ENST00000441883.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.357G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1084G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+424G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.339G>A
  hgvsp: ENST00000450882.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.355G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.339G>A
  hgvsp: ENST00000447696.1:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.339G>A
  hgvsp: ENST00000389675.2:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.337G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.339G>A
  hgvsp: ENST00000199706.8:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu113Glu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-419174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419174
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419174
    reference: chr 16
allele count: 4
allele frequency: 3.298316209575012e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.335G>A
  hgvsp: ENSP00000199706.7:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+420G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1080G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.335G>A
  hgvsp: ENSP00000374326.2:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.335G>A
  hgvsp: ENSP00000390399.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.333G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.335G>A
  hgvsp: ENSP00000395305.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.335G>A
  hgvsp: ENSP00000398684.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.351G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.353G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg112Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

16-419175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419175
    reference: chr 16
allele count: 4
allele frequency: 3.298642608566575e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.334C>T
  hgvsp: ENSP00000374326.2:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.334C>T
  hgvsp: ENSP00000199706.7:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.334C>T
  hgvsp: ENSP00000395305.1:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.332C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1079C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.334C>T
  hgvsp: ENSP00000390399.1:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.334C>T
  hgvsp: ENSP00000398684.1:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.352C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+419C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Arg112Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-419175-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419175
    reference: chr 16
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.352C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.334C>A
  hgvsp: ENST00000447696.1:c.334C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.334C>A
  hgvsp: ENST00000199706.8:c.334C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+419C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.332C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.334C>A
  hgvsp: ENST00000450882.1:c.334C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.334C>A
  hgvsp: ENST00000441883.1:c.334C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1079C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.350C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.334C>A
  hgvsp: ENST00000389675.2:c.334C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg112Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/16-419183-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419183
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419183
    reference: chr 16
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.326T>G
  hgvsp: ENSP00000395305.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1071T>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.326T>G
  hgvsp: ENSP00000398684.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.326T>G
  hgvsp: ENSP00000390399.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.326T>G
  hgvsp: ENSP00000374326.2:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+411T>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.344T>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.342T>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.324T>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.326T>G
  hgvsp: ENSP00000199706.7:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu109Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

16-419184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419184
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419184
    reference: chr 16
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.325C>T
  hgvsp: ENST00000450882.1:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+410C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.325C>T
  hgvsp: ENST00000441883.1:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.323C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1070C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.325C>T
  hgvsp: ENST00000447696.1:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.343C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.325C>T
  hgvsp: ENST00000389675.2:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.325C>T
  hgvsp: ENST00000199706.8:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.341C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu109Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

16-419185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419185
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419185
    reference: chr 16
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.324G>A
  hgvsp: ENST00000199706.8:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1069G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.324G>A
  hgvsp: ENST00000441883.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.324G>A
  hgvsp: ENST00000447696.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.324G>A
  hgvsp: ENST00000450882.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.324G>A
  hgvsp: ENST00000389675.2:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.342G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.322G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+409G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.340G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln108Gln
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

16-419186-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419186
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419186
    reference: chr 16
allele count: 3
allele frequency: 2.474716644944154e-5
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1068A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.323A>G
  hgvsp: ENSP00000374326.2:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.341A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.339A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.323A>G
  hgvsp: ENSP00000199706.7:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.323A>G
  hgvsp: ENSP00000395305.1:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.321A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.323A>G
  hgvsp: ENSP00000398684.1:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.323A>G
  hgvsp: ENSP00000390399.1:p.Gln108Arg
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+408A>G
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln108Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

16-419194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419194
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419194
    reference: chr 16
allele count: 5
allele frequency: 4.127047015319599e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+400G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.315G>A
  hgvsp: ENSP00000398684.1:p.Trp105Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.315G>A
  hgvsp: ENSP00000199706.7:p.Trp105Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.331G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.315G>A
  hgvsp: ENSP00000395305.1:p.Trp105Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.315G>A
  hgvsp: ENSP00000390399.1:p.Trp105Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1060G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.333G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.315G>A
  hgvsp: ENSP00000374326.2:p.Trp105Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.313G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp105Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-419198-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419198
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419198
    reference: chr 16
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.311T>A
  hgvsp: ENSP00000374326.2:p.Val104Glu
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+396T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.327T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1056T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.311T>A
  hgvsp: ENSP00000395305.1:p.Val104Glu
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.311T>A
  hgvsp: ENSP00000390399.1:p.Val104Glu
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.309T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.329T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.311T>A
  hgvsp: ENSP00000199706.7:p.Val104Glu
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.311T>A
  hgvsp: ENSP00000398684.1:p.Val104Glu
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val104Glu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-419203-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419203
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419203
    reference: chr 16
allele count: 16
allele frequency: 1.320611443098154e-4
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.306G>A
  hgvsp: ENST00000199706.8:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.304G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.306G>A
  hgvsp: ENST00000450882.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.306G>A
  hgvsp: ENST00000389675.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.306G>A
  hgvsp: ENST00000447696.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.324G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.322G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.306G>A
  hgvsp: ENST00000441883.1:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1051G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+391G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys102Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-419208-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419208
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419208
    reference: chr 16
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.301C>G
  hgvsp: ENSP00000390399.1:p.Leu101Val
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1046C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.299C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.301C>G
  hgvsp: ENSP00000398684.1:p.Leu101Val
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.301C>G
  hgvsp: ENSP00000374326.2:p.Leu101Val
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.319C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.301C>G
  hgvsp: ENSP00000199706.7:p.Leu101Val
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+386C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.301C>G
  hgvsp: ENSP00000395305.1:p.Leu101Val
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.317C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu101Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

16-419209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419209
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419209
    reference: chr 16
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.300G>A
  hgvsp: ENST00000447696.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.300G>A
  hgvsp: ENST00000450882.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.300G>A
  hgvsp: ENST00000389675.2:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+385G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.316G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.300G>A
  hgvsp: ENST00000199706.8:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.298G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.318G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.300G>A
  hgvsp: ENST00000441883.1:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1045G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
hgvs: n.298G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-419210-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419210
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419210
    reference: chr 16
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.315G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.317G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.299G>A
  hgvsp: ENSP00000199706.7:p.Arg100Lys
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.299G>A
  hgvsp: ENSP00000398684.1:p.Arg100Lys
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.297G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.299G>A
  hgvsp: ENSP00000374326.2:p.Arg100Lys
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.299G>A
  hgvsp: ENSP00000395305.1:p.Arg100Lys
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.299G>A
  hgvsp: ENSP00000390399.1:p.Arg100Lys
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1044G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+384G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg100Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-419217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419217
    reference: chr 16
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.292T>C
  hgvsp: ENSP00000395305.1:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.292T>C
  hgvsp: ENSP00000374326.2:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.292T>C
  hgvsp: ENSP00000199706.7:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-6T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.310T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.292T>C
  hgvsp: ENSP00000398684.1:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.292T>C
  hgvsp: ENSP00000390399.1:p.Ser98Pro
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.308T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1037T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+377T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser98Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

16-419218-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419218
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419218
    reference: chr 16
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.307C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.291C>G
  hgvsp: ENST00000199706.8:c.291C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.291C>G
  hgvsp: ENST00000447696.1:c.291C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.291C>G
  hgvsp: ENST00000450882.1:c.291C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1036C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.291C>G
  hgvsp: ENST00000441883.1:c.291C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.309C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+376C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.291C>G
  hgvsp: ENST00000389675.2:c.291C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-7C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.291C>G
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-419220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419220
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419220
    reference: chr 16
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1034C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289C>T
  hgvsp: ENSP00000398684.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289C>T
  hgvsp: ENSP00000199706.7:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289C>T
  hgvsp: ENSP00000390399.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289C>T
  hgvsp: ENSP00000395305.1:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289C>T
  hgvsp: ENSP00000374326.2:p.Leu97Phe
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+374C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu97Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

16-419222-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419222
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419222
    reference: chr 16
allele count: 2
allele frequency: 1.652264428399121e-5
allele num: 121046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1032A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-11A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-2A>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+372A>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
hgvs: c.289-2A>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

16-419223-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419223
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419223
    reference: chr 16
allele count: 3
allele frequency: 2.478560452089426e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-12C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1031C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+371C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-3C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-3C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
hgvs: c.289-3C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

16-419225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419225
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419225
    reference: chr 16
allele count: 2
allele frequency: 1.652837922713299e-5
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1029C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-14C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-5C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+369C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-5C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: c.289-5C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-419227-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419227
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419227
    reference: chr 16
allele count: 1
allele frequency: 8.264462809917356e-6
allele num: 121000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+367C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-16C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-7C>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1027C>A
  variant of: http://identifiers.org/hgnc/14484
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 8.25e1
  variant carriers: 0
hgvs: c.289-7C>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

16-419229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419229
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419229
    reference: chr 16
allele count: 2
allele frequency: 1.653329806229747e-5
allele num: 120968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-18C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1025C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+365C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-9C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-9C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13216
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

16-419233-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419233
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419233
    reference: chr 16
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-22G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-13G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+361G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-13G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2928
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-419237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419237
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419237
    reference: chr 16
allele count: 2
allele frequency: 1.654177625593436e-5
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+357C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-26C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-17C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1017C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-17C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

16-419237-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419237
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419237
    reference: chr 16
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1017C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+357C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-26C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-17C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-17C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-419244-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419244
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419244
    reference: chr 16
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1010A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+350A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-33A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-24A>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-24A>G
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

16-419244-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419244
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419244
    reference: chr 16
allele count: 3
allele frequency: 2.483649308717609e-5
allele num: 120790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-33A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1010A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-24A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+350A>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-24A>C
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2888
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-419246-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419246
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419246
    reference: chr 16
allele count: 4
allele frequency: 3.311477581296774e-5
allele num: 120792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-35T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.1008T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+348T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-26T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-26T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-419255-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419255
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419255
    reference: chr 16
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.999C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+339C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-44C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-35C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-35C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-419266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419266
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419266
    reference: chr 16
allele count: 4
allele frequency: 3.550821127385708e-5
allele num: 112650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+328G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.988G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-55G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-46G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-46G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

16-419267-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419267
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419267
    reference: chr 16
allele count: 1
allele frequency: 9.003979759053502e-6
allele num: 111062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-56T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.987T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-47T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+327T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5332
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

16-419267-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419267
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419267
    reference: chr 16
allele count: 124
allele frequency: 1.116493490122634e-3
allele num: 111062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-56T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.987T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+327T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-47T>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-47T>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6159
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

16-419269-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419269
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419269
    reference: chr 16
allele count: 1
allele frequency: 9.394258229370209e-6
allele num: 106448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+325T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-58T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-49T>C
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.985T>C
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6917
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15321
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6031
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-419270-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419270
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419270
    reference: chr 16
allele count: 2
allele frequency: 2.455192732629511e-5
allele num: 81460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+324G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-59G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.984G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-50G>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-50G>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12856
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-419271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419271
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419271
    reference: chr 16
allele count: 1
allele frequency: 1.227777232099008e-5
allele num: 81448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.983G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-60G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-51G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+323G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8954
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6097
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

16-419570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419570
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419570
    reference: chr 16
allele count: 1
allele frequency: 6.269592476489028e-5
allele num: 15950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.684C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-350C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.296-359C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+24C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-350C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5536
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

16-419575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419575
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419575
    reference: chr 16
allele count: 5
allele frequency: 3.092145949288807e-4
allele num: 16170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.289-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.61+19C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.679C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.295+356C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.289-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.289-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.289-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.305-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.307-355C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.289-355C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

16-419597-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419597
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419597
    reference: chr 16
allele count: 18
allele frequency: 1.204335608189482e-3
allele num: 14946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.58C>G
  hgvsp: ENSP00000414038.1:p.Arg20Gly
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.657C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.288+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.288+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.288+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.304+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.288+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.288+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.306+334C>G
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.295+334C>G
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4625
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg20Gly
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

16-419599-A-AGCTCTGCTCGCCTCCCCCACCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419599
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419621
    reference: chr 16
allele count: 8
allele frequency: 5.331911490269261e-4
allele num: 15004
alternate allele: AGCTCTGCTCGCCTCCCCCACCT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsp: ENSP00000414038.1:p.Leu19GlnfsTer?
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4671
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu19GlnfsTer?
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-419599-AGCTCTGCTCGCCTCCCCCACCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419599
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419577
    reference: chr 16
allele count: 66
allele frequency: 4.398826979472141e-3
allele num: 15004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsp: ENSP00000414038.1:p.Arg12PhefsTer?
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7455
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2556
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6345
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg12PhefsTer?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: AGCTCTGCTCGCCTCCCCCACCT
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-419608-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419608
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419608
    reference: chr 16
allele count: 2
allele frequency: 1.132502831257078e-4
allele num: 17660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.47G>A
  hgvsp: ENSP00000414038.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.304+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.306+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.288+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.288+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.646G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.288+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.288+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.288+323G>A
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.295+323G>A
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg16Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-419609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 419609
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 419609
    reference: chr 16
allele count: 13
allele frequency: 7.376305038583749e-4
allele num: 17624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000483764
  gene symbol: MRPL28
  hgvsc: ENST00000483764.1:n.306+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000390399
  ensembl transcript: ENST00000447696
  gene symbol: MRPL28
  hgvsc: ENST00000447696.1:c.288+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000395305
  ensembl transcript: ENST00000450882
  gene symbol: MRPL28
  hgvsc: ENST00000450882.1:c.288+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000374326
  ensembl transcript: ENST00000389675
  gene symbol: MRPL28
  hgvsc: ENST00000389675.2:c.288+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000461550
  gene symbol: MRPL28
  hgvsc: ENST00000461550.1:n.295+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000481453
  gene symbol: MRPL28
  hgvsc: ENST00000481453.1:n.645C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000414038
  ensembl transcript: ENST00000429738
  gene symbol: MRPL28
  hgvsc: ENST00000429738.1:c.46C>T
  hgvsp: ENSP00000414038.1:p.Arg16Ter
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000398684
  ensembl transcript: ENST00000441883
  gene symbol: MRPL28
  hgvsc: ENST00000441883.1:c.288+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl protein: ENSP00000199706
  ensembl transcript: ENST00000199706
  gene symbol: MRPL28
  hgvsc: ENST00000199706.8:c.288+322C>T
  variant of: http://identifiers.org/hgnc/14484
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000086504
  ensembl transcript: ENST00000469744
  gene symbol: MRPL28
  hgvsc: ENST00000469744.1:n.304+322C>T
  variant of: http://identifiers.org/hgnc/14484
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg16Ter
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 4307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4701
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

DP
type: SiteQuality
SIO_000300: 1.674088e6

QD
type: SiteQuality
SIO_000300: 2.18e1

VQSLOD
type: SiteQuality
SIO_000300: -1.771e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.024e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4706
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.02e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.53e-1

DP
type: SiteQuality
SIO_000300: 1.67495e6

FS
type: SiteQuality
SIO_000300: 7.982e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33369
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8552
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3018
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.205690860863275e-4
allele num: 66352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.921e1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

DP
type: SiteQuality
SIO_000300: 1.676329e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 21

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 59

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 34

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1538
bin: 6.75e1
variant carriers: 126

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 34

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 298

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 7258
bin: 6.25e1
variant carriers: 73

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 40

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 5

GenotypeQuality
all individuals: 400
bin: 7.25e1
variant carriers: 78

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 179

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 63

GenotypeQuality
all individuals: 49558
bin: 9.75e1
variant carriers: 49499

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 49

GenotypeQuality
all individuals: 452
bin: 7.75e1
variant carriers: 164

European (Non-Finnish)
type: Population
allele count: 37403
allele frequency: 5.62282020444979e-1
allele num: 66520
num of homozygotes: 10652

East Asian
type: Population
allele count: 4863
allele frequency: 5.629775410974762e-1
allele num: 8638
num of homozygotes: 1368

European (Finnish)
type: Population
allele count: 3827
allele frequency: 5.798484848484848e-1
allele num: 6600
num of homozygotes: 1125

South Asian
type: Population
allele count: 11927
allele frequency: 7.225857264025203e-1
allele num: 16506
num of homozygotes: 4349

African
type: Population
allele count: 8975
allele frequency: 8.646435452793835e-1
allele num: 10380
num of homozygotes: 3877

Latino
type: Population
allele count: 7146
allele frequency: 6.188084516799446e-1
allele num: 11548
num of homozygotes: 2215

Other
type: Population
allele count: 530
allele frequency: 5.849889624724062e-1
allele num: 906
num of homozygotes: 154

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

FS
type: SiteQuality
SIO_000300: 5.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

QD
type: SiteQuality
SIO_000300: 2.232e1

DP
type: SiteQuality
SIO_000300: 3.672929e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.625e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14567
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28226
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.994e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.211e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -1.124e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.163819e6

QD
type: SiteQuality
SIO_000300: 1.668e1

GenotypeQuality
all individuals: 515
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10018
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14566
bin: 9.75e1
variant carriers: 5

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.42e-1

QD
type: SiteQuality
SIO_000300: 2.899e1

DP
type: SiteQuality
SIO_000300: 3.164062e6

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.552e0

VQSLOD
type: SiteQuality
SIO_000300: -1.51e0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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DP
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ClippingRankSum
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FS
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MQRankSum
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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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GenotypeQuality
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African
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Latino
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Other
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East Asian
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FS
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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European (Non-Finnish)
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allele num: 66594
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Latino
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Other
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East Asian
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African
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South Asian
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European (Finnish)
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VQSLOD
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ClippingRankSum
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QD
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16512
num of homozygotes: 0

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

African
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European (Non-Finnish)
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Other
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East Asian
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South Asian
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Latino
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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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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European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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Latino
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African
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Other
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FS
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DP
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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South Asian
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.42e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 11

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: 3.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1327
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variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.050987928652934e-4
allele num: 66604
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

QD
type: SiteQuality
SIO_000300: 1.302e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.42e-1

DP
type: SiteQuality
SIO_000300: 3.165946e6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 3.16581e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

FS
type: SiteQuality
SIO_000300: 3.895e0

QD
type: SiteQuality
SIO_000300: 1.385e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.145e0

VQSLOD
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.573e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

DP
type: SiteQuality
SIO_000300: 3.16588e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.43e-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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variant carriers: 6

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.006845202353788e-5
allele num: 66616
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.419e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.839e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

FS
type: SiteQuality
SIO_000300: 4.602e0

DP
type: SiteQuality
SIO_000300: 3.16603e6

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 25
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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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

DP
type: SiteQuality
SIO_000300: 3.166095e6

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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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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
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allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.05e-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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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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Latino
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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.502881844380403e-5
allele num: 66624
num of homozygotes: 0

Other
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MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.927e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.561e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.211e0

DP
type: SiteQuality
SIO_000300: 3.16652e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.195e1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14514
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1332
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28574
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.294e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.249e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.399e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.166523e6

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.781e1

GenotypeQuality
all individuals: 427
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1101
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 28407
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9907
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 15895
bin: 9.75e1
variant carriers: 15363

GenotypeQuality
all individuals: 338
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2179
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2272
bin: 7.75e1
variant carriers: 6

East Asian
type: Population
allele count: 1259
allele frequency: 1.45751331326696e-1
allele num: 8638
num of homozygotes: 93

African
type: Population
allele count: 364
allele frequency: 3.506743737957611e-2
allele num: 10380
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 10684
allele frequency: 1.603193181477147e-1
allele num: 66642
num of homozygotes: 873

Other
type: Population
allele count: 131
allele frequency: 1.44273127753304e-1
allele num: 908
num of homozygotes: 8

South Asian
type: Population
allele count: 2700
allele frequency: 1.635174418604651e-1
allele num: 16512
num of homozygotes: 231

European (Finnish)
type: Population
allele count: 849
allele frequency: 1.283640762019958e-1
allele num: 6614
num of homozygotes: 48

Latino
type: Population
allele count: 719
allele frequency: 6.215421853388658e-2
allele num: 11568
num of homozygotes: 42

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.594e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

DP
type: SiteQuality
SIO_000300: 3.686231e6

QD
type: SiteQuality
SIO_000300: 1.452e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13545
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3024
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3037
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.040175e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37717
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1441
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.206e1

DP
type: SiteQuality
SIO_000300: 3.040083e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 8.316000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37715
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

DP
type: SiteQuality
SIO_000300: 3.039973e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

QD
type: SiteQuality
SIO_000300: 1.589e1

FS
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37717
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13539
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.039946e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 9.66e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.609e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 3022
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variant carriers: 0

GenotypeQuality
all individuals: 37712
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1443
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variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 3031
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 566
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 9.75e1
variant carriers: 4

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

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

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

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

DP
type: SiteQuality
SIO_000300: 3.039909e6

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeQuality
all individuals: 3031
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37690
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.503017021404341e-5
allele num: 66622
num of homozygotes: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.46e-1

FS
type: SiteQuality
SIO_000300: 2.452e0

QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.55e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

DP
type: SiteQuality
SIO_000300: 3.039512e6

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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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.46e-1

ReadPosRankSum
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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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SIO_000300: 2.452e0

MQRankSum
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SIO_000300: 2.4e-1

MQ
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00228173411793e-5
allele num: 66616
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.805e0

QD
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SIO_000300: 9.49e0

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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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.339e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 3.038808e6

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

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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GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
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

ClippingRankSum
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SIO_000300: 3.46e-1

QD
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DP
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BaseQRankSum
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FS
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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MQRankSum
type: SiteQuality
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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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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele frequency: 3.029385034837928e-4
allele num: 6602
num of homozygotes: 0

Other
type: Population
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.004536850644473e-5
allele num: 66566
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African
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allele num: 10360
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South Asian
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QD
type: SiteQuality
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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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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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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Latino
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allele frequency: 8.643042350907519e-5
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11568
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African
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allele frequency: 0.0e0
allele num: 10364
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European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.802288906911778e-4
allele num: 66582
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.821272462360369e-4
allele num: 16472
num of homozygotes: 0

MQ
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SIO_000300: 5.956e1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -3.15e-1

BaseQRankSum
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QD
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MQRankSum
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SIO_000300: -1.4e-1

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -9.086e-1

DP
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.987e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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MQ
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

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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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

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

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

Other
type: Population
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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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MQRankSum
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SIO_000300: 1.1e0

MQ
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SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

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

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.15e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.84e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10362
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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 6.086427267194157e-5
allele num: 16430
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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FS
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QD
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ReadPosRankSum
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SIO_000300: -1.33e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
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European (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: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

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

Latino
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European (Non-Finnish)
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East Asian
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allele num: 8652
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African
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South Asian
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Other
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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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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South Asian
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European (Non-Finnish)
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African
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Other
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East Asian
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Latino
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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DP
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SIO_000300: 3.021856e6

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 6.037e1

GenotypeQuality
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variant carriers: 3

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.005710850616171e-5
allele num: 66540
num of homozygotes: 0

African
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Other
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allele frequency: 0.0e0
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East Asian
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MQ
type: SiteQuality
SIO_000300: 6.053e1

VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 8.691000000000001e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.98e-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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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.503081316699233e-5
allele num: 66530
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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: -1.907e0

InbreedingCoeff
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SIO_000300: -3.0e-4

VQSLOD
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FS
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QD
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ClippingRankSum
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.998e1

DP
type: SiteQuality
SIO_000300: 3.018356e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-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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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 9.648784253184099e-5
allele num: 10364
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 count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66532
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Other
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ClippingRankSum
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SIO_000300: -1.639e0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.033e1

MQRankSum
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SIO_000300: -9.3e-2

DP
type: SiteQuality
SIO_000300: 3.016016e6

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
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South Asian
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allele count: 2
allele frequency: 1.223391240518718e-4
allele num: 16348
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 3.014858e6

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.997e1

InbreedingCoeff
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SIO_000300: -3.0e-4

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.659e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8652
num of homozygotes: 0

South Asian
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allele frequency: 6.12369871402327e-5
allele num: 16330
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 (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: 0
allele frequency: 0.0e0
allele num: 66486
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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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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South Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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MQ
type: SiteQuality
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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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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variant carriers: 0

European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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African
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Latino
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Other
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ReadPosRankSum
type: SiteQuality
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FS
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QD
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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African
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Latino
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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DP
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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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SIO_000300: 1.71e0

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12844
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 2.989218e6

MQ
type: SiteQuality
SIO_000300: 6.038e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 2.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

MQ
type: SiteQuality
SIO_000300: 6.017e1

QD
type: SiteQuality
SIO_000300: 1.276e1

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

FS
type: SiteQuality
SIO_000300: 4.851e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.988722e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.36e-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
all individuals: 7
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.251562890722681e-5
allele num: 15996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.768e0

DP
type: SiteQuality
SIO_000300: 2.971382e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

QD
type: SiteQuality
SIO_000300: 1.009e1

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173984503404555e-4
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.322237017310254e-5
allele num: 12016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.027163997567403e-4
allele num: 9866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.664e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

MQ
type: SiteQuality
SIO_000300: 6.036e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.038e0

DP
type: SiteQuality
SIO_000300: 2.92073e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4147
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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
all individuals: 1209
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.591241805104704e-5
allele num: 62844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.92523e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.996e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 124

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2203
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variant carriers: 0

GenotypeQuality
all individuals: 6755
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 75
allele frequency: 1.147490820073439e-2
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.051282051282051e-4
allele num: 9750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.478836483992107e-4
allele num: 62844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.996e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 2.92523e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-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
all individuals: 602
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variant carriers: 1

GenotypeQuality
all individuals: 399
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.646415752905924e-5
allele num: 60738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.472e0

MQ
type: SiteQuality
SIO_000300: 5.88e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 2.955305e6

VQSLOD
type: SiteQuality
SIO_000300: -8.484e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.55e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
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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: 1725
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GenotypeQuality
all individuals: 8954
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GenotypeQuality
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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: 6097
bin: 3.75e1
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GenotypeQuality
all individuals: 2054
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.079765937788728e-4
allele num: 6494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 8.808999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.798e-1

QD
type: SiteQuality
SIO_000300: 1.521e1

MQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

DP
type: SiteQuality
SIO_000300: 3.001493e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.485e0

GenotypeQuality
all individuals: 12851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 2546
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GenotypeQuality
all individuals: 1732
bin: 2.5e0
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GenotypeQuality
all individuals: 7733
bin: 1.75e1
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GenotypeQuality
all individuals: 71
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4704
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.001352e6

QD
type: SiteQuality
SIO_000300: 1.394e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.667e0

VQSLOD
type: SiteQuality
SIO_000300: -1.975e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.78e0

FS
type: SiteQuality
SIO_000300: 7.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: -2.143e0

MQ
type: SiteQuality
SIO_000300: 6.042e1

GenotypeQuality
all individuals: 70
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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: 4.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 926
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.506024096385542e-4
allele num: 6640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.54336e5

VQSLOD
type: SiteQuality
SIO_000300: -1.077e0

QD
type: SiteQuality
SIO_000300: 1.079e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.256e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.56e-2

MQ
type: SiteQuality
SIO_000300: 5.638e1

GenotypeQuality
all individuals: 1492
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
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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bin: 3.75e1
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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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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 218
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 7.378984651711924e-4
allele num: 6776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-2

QD
type: SiteQuality
SIO_000300: 1.061e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.218e0

DP
type: SiteQuality
SIO_000300: 2.64657e5

FS
type: SiteQuality
SIO_000300: 9.978999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.088e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
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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: 166
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6372
bin: 7.5e0
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 808
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6650
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.617977528089887e-3
allele num: 178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 8.795669824086604e-3
allele num: 1478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.716049382716049e-4
allele num: 5184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 672
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

FS
type: SiteQuality
SIO_000300: 1.124e0

DP
type: SiteQuality
SIO_000300: 3.05223e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.98e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 1.367e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6345
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 865
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 654
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 5.555555555555556e-3
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.76923076923077e-4
allele num: 5200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.968367651447329e-4
allele num: 6702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 3.06342e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.82e-2

FS
type: SiteQuality
SIO_000300: 1.125e0

MQ
type: SiteQuality
SIO_000300: 5.329e1

VQSLOD
type: SiteQuality
SIO_000300: -1.921e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.489e0

QD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 654
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4671
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GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 865
bin: 9.75e1
variant carriers: 66

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.923076923076923e-4
allele num: 5200
num of homozygotes: 0

South Asian
type: Population
allele count: 62
allele frequency: 9.250969859743359e-3
allele num: 6702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.575757575757576e-3
allele num: 264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.555555555555556e-3
allele num: 180
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.329e1

FS
type: SiteQuality
SIO_000300: 1.125e0

QD
type: SiteQuality
SIO_000300: 1.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.489e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.82e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.921e-1

DP
type: SiteQuality
SIO_000300: 3.06342e5

GenotypeQuality
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
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GenotypeQuality
all individuals: 4831
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variant carriers: 0

GenotypeQuality
all individuals: 256
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variant carriers: 0

GenotypeQuality
all individuals: 254
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 2.25e1
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GenotypeQuality
all individuals: 7300
bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 730
bin: 6.75e1
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 83
bin: 4.75e1
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GenotypeQuality
all individuals: 1489
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variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1126
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.724053391446472e-4
allele num: 7342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.87e-2

FS
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.865e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.09065e5

QD
type: SiteQuality
SIO_000300: 7.6e0