8-125570972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125570972
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125570972
    reference: chr 8
allele count: 1
allele frequency: 4.246284501061571e-5
allele num: 23550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2326C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.379C>T
  hgvsp: ENST00000519168.1:c.379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-856C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1137C>T
  hgvsp: ENST00000378017.3:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2377C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-856C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-856C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8916G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2377C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-856C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.339C>T
  hgvsp: ENST00000395508.2:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-856C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-856C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala127Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-125570990-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125570990
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125570990
    reference: chr 8
allele count: 2
allele frequency: 6.181233774261343e-5
allele num: 32356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.321G>T
  hgvsp: ENST00000395508.2:c.321G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2344G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-874G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2395G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-874G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8898C>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2395G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-874G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-874G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1119G>T
  hgvsp: ENST00000378017.3:c.1119G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.361G>T
  hgvsp: ENST00000519168.1:c.361G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-874G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-874G>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9986
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser121Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

8-125570991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125570991
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125570991
    reference: chr 8
allele count: 2
allele frequency: 6.076441635778088e-5
allele num: 32914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-875C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-875C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.320C>T
  hgvsp: ENSP00000378884.2:p.Ser107Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-875C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-875C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1118C>T
  hgvsp: ENSP00000367256.3:p.Ser373Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-875C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2396C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.360C>T
  hgvsp: ENSP00000428685.1:p.Ser121Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2345C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2396C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8897G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-875C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35070
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser121Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

8-125570993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125570993
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125570993
    reference: chr 8
allele count: 1
allele frequency: 2.953162837398854e-5
allele num: 33862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2347C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1116C>T
  hgvsp: ENST00000378017.3:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-877C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.358C>T
  hgvsp: ENST00000519168.1:c.358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-877C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-877C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.318C>T
  hgvsp: ENST00000395508.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2398C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8895G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-877C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-877C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2398C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-877C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34937
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser120Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-125571005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571005
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571005
    reference: chr 8
allele count: 1
allele frequency: 2.710761724044456e-5
allele num: 36890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8883G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1104C>T
  hgvsp: ENST00000378017.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2359C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.346C>T
  hgvsp: ENST00000519168.1:c.346C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2410C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-889C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.306C>T
  hgvsp: ENST00000395508.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2410C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33742
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro116Pro
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-125571005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571005
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571005
    reference: chr 8
allele count: 4
allele frequency: 1.084304689617783e-4
allele num: 36890
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-889C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-889C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2359C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8883G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.306C>G
  hgvsp: ENST00000395508.2:c.306C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.346C>G
  hgvsp: ENST00000519168.1:c.346C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1104C>G
  hgvsp: ENST00000378017.3:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-889C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2410C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2410C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-889C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-889C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-889C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro116Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

8-125571014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571014
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571014
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 36830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-898C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-898C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2419C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1095C>T
  hgvsp: ENST00000378017.3:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-898C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.297C>T
  hgvsp: ENST00000395508.2:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.337C>T
  hgvsp: ENST00000519168.1:c.337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8874G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2368C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2419C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-898C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-898C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-898C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys113Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

8-125571021-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571021
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571021
    reference: chr 8
allele count: 1
allele frequency: 2.723163226403791e-5
allele num: 36722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1088G>C
  hgvsp: ENSP00000367256.3:p.Ser363Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2375G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2426G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.330G>C
  hgvsp: ENSP00000428685.1:p.Ser111Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.290G>C
  hgvsp: ENSP00000378884.2:p.Ser97Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8867C>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-905G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2426G>C
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser111Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

8-125571036-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571036
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571036
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 32988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-920C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1073C>A
  hgvsp: ENSP00000367256.3:p.Thr358Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-920C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2441C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2390C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-920C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-920C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8852G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.275C>A
  hgvsp: ENSP00000378884.2:p.Thr92Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.315C>A
  hgvsp: ENSP00000428685.1:p.Thr106Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2441C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-920C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-920C>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr106Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD

8-125571037-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571037
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571037
    reference: chr 8
allele count: 11
allele frequency: 3.795983159638346e-4
allele num: 28978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2442A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8851T>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.274A>C
  hgvsp: ENSP00000378884.2:p.Thr92Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.314A>C
  hgvsp: ENSP00000428685.1:p.Thr106Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2442A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1072A>C
  hgvsp: ENSP00000367256.3:p.Thr358Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-921A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2391A>C
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 30789
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11250
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr106Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-125571039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571039
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571039
    reference: chr 8
allele count: 1
allele frequency: 3.217089177712006e-5
allele num: 31084
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8849T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1070A>G
  hgvsp: ENSP00000367256.3:p.Glu357Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2444A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2444A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.272A>G
  hgvsp: ENSP00000378884.2:p.Glu91Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.312A>G
  hgvsp: ENSP00000428685.1:p.Glu105Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-923A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2393A>G
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu105Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

8-125571041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571041
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571041
    reference: chr 8
allele count: 5
allele frequency: 1.63036389722186e-4
allele num: 30668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.270G>A
  hgvsp: ENST00000395508.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.310G>A
  hgvsp: ENST00000519168.1:c.310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1068G>A
  hgvsp: ENST00000378017.3:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8847C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2395G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2446G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-925G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2446G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30934
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ser104Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

8-125571045-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571045
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571045
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 29868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-929C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-929C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.306C>G
  hgvsp: ENSP00000428685.1:p.Ala103Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-929C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.266C>G
  hgvsp: ENSP00000378884.2:p.Ala89Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2399C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2450C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-929C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1064C>G
  hgvsp: ENSP00000367256.3:p.Ala355Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-929C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8843G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2450C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-929C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30765
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala103Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-125571049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571049
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571049
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 28232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.302G>A
  hgvsp: ENSP00000428685.1:p.Glu102Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2454G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.262G>A
  hgvsp: ENSP00000378884.2:p.Glu88Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8839C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1060G>A
  hgvsp: ENSP00000367256.3:p.Glu354Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2454G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-933G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2403G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29673
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu102Lys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

8-125571059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571059
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571059
    reference: chr 8
allele count: 1
allele frequency: 4.009301579664822e-5
allele num: 24942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-943G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2464G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2413G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-943G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.252G>A
  hgvsp: ENST00000395508.2:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1050G>A
  hgvsp: ENST00000378017.3:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-943G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2464G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.292G>A
  hgvsp: ENST00000519168.1:c.292G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-943G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-943G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8829C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-943G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser98Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-125571068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571068
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571068
    reference: chr 8
allele count: 1
allele frequency: 4.250977724876721e-5
allele num: 23524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-952G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2473G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.243G>A
  hgvsp: ENST00000395508.2:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.283G>A
  hgvsp: ENST00000519168.1:c.283G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-952G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1041G>A
  hgvsp: ENST00000378017.3:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2422G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-952G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-952G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-952G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2473G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8820C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-952G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27072
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser95Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-125571069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571069
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571069
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 23008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.242C>T
  hgvsp: ENSP00000378884.2:p.Ser81Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2423C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-953C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8819G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.282C>T
  hgvsp: ENSP00000428685.1:p.Ser95Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1040C>T
  hgvsp: ENSP00000367256.3:p.Ser347Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-953C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2474C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2474C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-953C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-953C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-953C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-953C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser95Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-125571074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571074
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571074
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 22168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8814C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-1G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2479G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-1G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-1G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2479G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-958G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2428G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: splice acceptor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21363
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25527
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.278-1G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-125571081-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571081
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571081
    reference: chr 8
allele count: 1
allele frequency: 4.872344572208146e-5
allele num: 20524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2486T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2486T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8807A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-965T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2435T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.278-8T>C
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

8-125571093-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571093
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571093
    reference: chr 8
allele count: 1
allele frequency: 6.085686465433301e-5
allele num: 16432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8795A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-20T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-20T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-20T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2498T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2498T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-977T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2447T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18405
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS

8-125571094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571094
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571094
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 16352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-21G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2448G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2499G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-978G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8794C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-21G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2499G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-21G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18390
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-125571095-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571095
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571095
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 16434
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2500T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-22T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-22T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-22T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2500T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8793A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-979T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2449T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18360
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

8-125571096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571096
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571096
    reference: chr 8
allele count: 1
allele frequency: 6.270378730875344e-5
allele num: 15948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2450G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8792C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-23G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2501G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-980G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-23G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2501G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-23G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

8-125571097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571097
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571097
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 15782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-24C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2502C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-24C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-24C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2502C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8791G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-981C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2451C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 30273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17965
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

8-125571105-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571105
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571105
    reference: chr 8
allele count: 1
allele frequency: 7.23589001447178e-5
allele num: 13820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-32G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2510G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-32G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8783C>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-989G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2510G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-32G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2459G>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-125571108-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571108
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571108
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 13438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8780C>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-35G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-992G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-992G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-992G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2513G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-992G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-992G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-35G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-35G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2513G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2462G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-992G>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

8-125571116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125571116
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125571116
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 12402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1036-43C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.309-1000C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1048-1000C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-8772G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.436-1000C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-2521C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-2521C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-2470C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1036-1000C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.238-43C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.706-1000C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.278-43C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.271-1000C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16010
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31720
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

8-125574980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125574980
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125574980
    reference: chr 8
allele count: 38
allele frequency: 3.185621112284761e-4
allele num: 119286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435+43G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4908C>T
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23645
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15187
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

8-125574981-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125574981
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125574981
    reference: chr 8
allele count: 3
allele frequency: 2.512352399296541e-5
allele num: 119410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4907A>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435+42T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308+42T>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23721
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-125574982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125574982
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125574982
    reference: chr 8
allele count: 1
allele frequency: 8.379420144126027e-6
allele num: 119340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237+41G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4906C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308+41G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

8-125575013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575013
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575013
    reference: chr 8
allele count: 9126
allele frequency: 7.584269662921349e-2
allele num: 120328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4875G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435+10C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035+10C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 673
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 17239
  bin: 2.25e1
  variant carriers: 277
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 8.25e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 24428
  bin: 2.75e1
  variant carriers: 374
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 3.75e1
  variant carriers: 531
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.25e1
  variant carriers: 713
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 3.25e1
  variant carriers: 432
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 746
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.25e1
  variant carriers: 569
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.75e1
  variant carriers: 675
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.25e1
  variant carriers: 590
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.75e1
  variant carriers: 690
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 744
genotype quality: GenotypeQuality
num of homozygotes: 423
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-125575015-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575015
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575015
    reference: chr 8
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4873A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435+8T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035+8T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18988
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1035+8T>C
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

8-125575023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575023
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575023
    reference: chr 8
allele count: 8
allele frequency: 6.6333891643588e-5
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.435G>A
  hgvsp: ENST00000522118.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.577G>A
  hgvsp: ENST00000523179.1:c.577G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.237G>A
  hgvsp: ENST00000395508.2:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1035G>A
  hgvsp: ENST00000518547.1:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.435G>A
  hgvsp: ENST00000354184.4:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1035G>A
  hgvsp: ENST00000378017.3:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.277G>A
  hgvsp: ENST00000519168.1:c.277G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4865C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1047G>A
  hgvsp: ENST00000325064.5:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.705G>A
  hgvsp: ENST00000524090.1:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.435G>A
  hgvsp: ENST00000431961.2:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.270G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.308G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1035G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

8-125575026-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575026
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575026
    reference: chr 8
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.432C>G
  hgvsp: ENSP00000393606.2:p.Asn144Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.702C>G
  hgvsp: ENSP00000428319.1:p.Asn234Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.305C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1032C>G
  hgvsp: ENSP00000429064.1:p.Asn344Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.432C>G
  hgvsp: ENSP00000346119.4:p.Asn144Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4862G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.574C>G
  hgvsp: ENSP00000428348.1:p.Asn192Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.432C>G
  hgvsp: ENSP00000428145.1:p.Asn144Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.234C>G
  hgvsp: ENSP00000378884.2:p.Asn78Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1032C>G
  hgvsp: ENSP00000367256.3:p.Asn344Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.274C>G
  hgvsp: ENSP00000428685.1:p.Asn92Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1044C>G
  hgvsp: ENSP00000322804.5:p.Asn348Lys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.267C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn344Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-125575039-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575039
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575039
    reference: chr 8
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1019C>A
  hgvsp: ENSP00000429064.1:p.Pro340Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.689C>A
  hgvsp: ENSP00000428319.1:p.Pro230Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1019C>A
  hgvsp: ENSP00000367256.3:p.Pro340Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.419C>A
  hgvsp: ENSP00000428145.1:p.Pro140Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.261C>A
  hgvsp: ENSP00000428685.1:p.Pro88Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.292C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.221C>A
  hgvsp: ENSP00000378884.2:p.Pro74Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.419C>A
  hgvsp: ENSP00000346119.4:p.Pro140Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.419C>A
  hgvsp: ENSP00000393606.2:p.Pro140Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1031C>A
  hgvsp: ENSP00000322804.5:p.Pro344Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.254C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.561C>A
  hgvsp: ENSP00000428348.1:p.Pro188Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4849G>T
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro340Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-125575041-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575041
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575041
    reference: chr 8
allele count: 44
allele frequency: 3.641479764959033e-4
allele num: 120830
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1017G>T
  hgvsp: ENST00000518547.1:c.1017G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.219G>T
  hgvsp: ENST00000395508.2:c.219G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.259G>T
  hgvsp: ENST00000519168.1:c.259G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.417G>T
  hgvsp: ENST00000431961.2:c.417G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.687G>T
  hgvsp: ENST00000524090.1:c.687G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.559G>T
  hgvsp: ENST00000523179.1:c.559G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.417G>T
  hgvsp: ENST00000522118.1:c.417G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1029G>T
  hgvsp: ENST00000325064.5:c.1029G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.417G>T
  hgvsp: ENST00000354184.4:c.417G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.290G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1017G>T
  hgvsp: ENST00000378017.3:c.1017G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4847C>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.252G>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro339Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

8-125575041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575041
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575041
    reference: chr 8
allele count: 2
allele frequency: 1.655218074981379e-5
allele num: 120830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.252G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4847C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.687G>A
  hgvsp: ENST00000524090.1:c.687G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.417G>A
  hgvsp: ENST00000431961.2:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.259G>A
  hgvsp: ENST00000519168.1:c.259G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1017G>A
  hgvsp: ENST00000518547.1:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1017G>A
  hgvsp: ENST00000378017.3:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.290G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.417G>A
  hgvsp: ENST00000522118.1:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.219G>A
  hgvsp: ENST00000395508.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.559G>A
  hgvsp: ENST00000523179.1:c.559G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.417G>A
  hgvsp: ENST00000354184.4:c.417G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1029G>A
  hgvsp: ENST00000325064.5:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro339Pro
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

8-125575042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575042
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575042
    reference: chr 8
allele count: 4
allele frequency: 3.309395373465268e-5
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.258C>T
  hgvsp: ENSP00000428685.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.218C>T
  hgvsp: ENSP00000378884.2:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1016C>T
  hgvsp: ENSP00000367256.3:p.Pro339Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.416C>T
  hgvsp: ENSP00000393606.2:p.Pro139Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1016C>T
  hgvsp: ENSP00000429064.1:p.Pro339Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.251C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.416C>T
  hgvsp: ENSP00000346119.4:p.Pro139Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.686C>T
  hgvsp: ENSP00000428319.1:p.Pro229Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.558C>T
  hgvsp: ENSP00000428348.1:p.Pro187Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.416C>T
  hgvsp: ENSP00000428145.1:p.Pro139Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1028C>T
  hgvsp: ENSP00000322804.5:p.Pro343Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4846G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.289C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro339Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

8-125575047-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575047
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575047
    reference: chr 8
allele count: 2025
allele frequency: 1.673719707739611e-2
allele num: 120988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.411C>A
  hgvsp: ENST00000354184.4:c.411C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.213C>A
  hgvsp: ENST00000395508.2:c.213C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.246C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4841G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.411C>A
  hgvsp: ENST00000431961.2:c.411C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.681C>A
  hgvsp: ENST00000524090.1:c.681C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.253C>A
  hgvsp: ENST00000519168.1:c.253C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.553C>A
  hgvsp: ENST00000523179.1:c.553C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.284C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.411C>A
  hgvsp: ENST00000522118.1:c.411C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1011C>A
  hgvsp: ENST00000378017.3:c.1011C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1011C>A
  hgvsp: ENST00000518547.1:c.1011C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1023C>A
  hgvsp: ENST00000325064.5:c.1023C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 19060
  bin: 2.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 29025
  bin: 2.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 125
genotype quality: GenotypeQuality
hgvs: p.Pro337Pro
num of homozygotes: 144
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

8-125575049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575049
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575049
    reference: chr 8
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.551C>T
  hgvsp: ENSP00000428348.1:p.Pro185Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.409C>T
  hgvsp: ENSP00000393606.2:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.409C>T
  hgvsp: ENSP00000428145.1:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.251C>T
  hgvsp: ENSP00000428685.1:p.Pro85Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.244C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1009C>T
  hgvsp: ENSP00000367256.3:p.Pro337Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1009C>T
  hgvsp: ENSP00000429064.1:p.Pro337Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.211C>T
  hgvsp: ENSP00000378884.2:p.Pro71Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.282C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.409C>T
  hgvsp: ENSP00000346119.4:p.Pro137Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1021C>T
  hgvsp: ENSP00000322804.5:p.Pro341Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.679C>T
  hgvsp: ENSP00000428319.1:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4839G>A
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro337Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-125575052-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575052
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575052
    reference: chr 8
allele count: 7
allele frequency: 5.782065684266174e-5
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1006T>A
  hgvsp: ENSP00000429064.1:p.Ser336Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.406T>A
  hgvsp: ENSP00000428145.1:p.Ser136Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1006T>A
  hgvsp: ENSP00000367256.3:p.Ser336Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.208T>A
  hgvsp: ENSP00000378884.2:p.Ser70Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.406T>A
  hgvsp: ENSP00000346119.4:p.Ser136Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.241T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.548T>A
  hgvsp: ENSP00000428348.1:p.Ser184Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1018T>A
  hgvsp: ENSP00000322804.5:p.Ser340Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.248T>A
  hgvsp: ENSP00000428685.1:p.Ser84Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.406T>A
  hgvsp: ENSP00000393606.2:p.Ser136Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.279T>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.676T>A
  hgvsp: ENSP00000428319.1:p.Ser226Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4836A>T
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser336Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-125575056-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575056
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575056
    reference: chr 8
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4832T>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1002A>T
  hgvsp: ENST00000378017.3:c.1002A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.275A>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1002A>T
  hgvsp: ENST00000518547.1:c.1002A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.244A>T
  hgvsp: ENST00000519168.1:c.244A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.204A>T
  hgvsp: ENST00000395508.2:c.204A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.402A>T
  hgvsp: ENST00000431961.2:c.402A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.402A>T
  hgvsp: ENST00000522118.1:c.402A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.672A>T
  hgvsp: ENST00000524090.1:c.672A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1014A>T
  hgvsp: ENST00000325064.5:c.1014A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.544A>T
  hgvsp: ENST00000523179.1:c.544A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.237A>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.402A>T
  hgvsp: ENST00000354184.4:c.402A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser334Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

8-125575062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575062
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575062
    reference: chr 8
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.269C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.396C>T
  hgvsp: ENST00000354184.4:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4826G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.996C>T
  hgvsp: ENST00000378017.3:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1008C>T
  hgvsp: ENST00000325064.5:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.198C>T
  hgvsp: ENST00000395508.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.396C>T
  hgvsp: ENST00000431961.2:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.996C>T
  hgvsp: ENST00000518547.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.538C>T
  hgvsp: ENST00000523179.1:c.538C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.238C>T
  hgvsp: ENST00000519168.1:c.238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.231C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.396C>T
  hgvsp: ENST00000522118.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.666C>T
  hgvsp: ENST00000524090.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser332Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-125575073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575073
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575073
    reference: chr 8
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.220G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.385G>A
  hgvsp: ENSP00000428145.1:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.985G>A
  hgvsp: ENSP00000367256.3:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.385G>A
  hgvsp: ENSP00000393606.2:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.655G>A
  hgvsp: ENSP00000428319.1:p.Ala219Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.227G>A
  hgvsp: ENSP00000428685.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.258G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.997G>A
  hgvsp: ENSP00000322804.5:p.Ala333Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.187G>A
  hgvsp: ENSP00000378884.2:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.527G>A
  hgvsp: ENSP00000428348.1:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.385G>A
  hgvsp: ENSP00000346119.4:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4815C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.985G>A
  hgvsp: ENSP00000429064.1:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala329Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-125575084-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575084
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575084
    reference: chr 8
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.974T>C
  hgvsp: ENSP00000429064.1:p.Ile325Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.374T>C
  hgvsp: ENSP00000428145.1:p.Ile125Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.374T>C
  hgvsp: ENSP00000393606.2:p.Ile125Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.974T>C
  hgvsp: ENSP00000367256.3:p.Ile325Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.216T>C
  hgvsp: ENSP00000428685.1:p.Ile73Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.644T>C
  hgvsp: ENSP00000428319.1:p.Ile215Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.247T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.374T>C
  hgvsp: ENSP00000346119.4:p.Ile125Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.516T>C
  hgvsp: ENSP00000428348.1:p.Ile173Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.176T>C
  hgvsp: ENSP00000378884.2:p.Ile59Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.986T>C
  hgvsp: ENSP00000322804.5:p.Ile329Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.209T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4804A>G
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile325Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

8-125575100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575100
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575100
    reference: chr 8
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.231C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.160C>T
  hgvsp: ENSP00000378884.2:p.His54Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.628C>T
  hgvsp: ENSP00000428319.1:p.His210Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.358C>T
  hgvsp: ENSP00000393606.2:p.His120Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.358C>T
  hgvsp: ENSP00000428145.1:p.His120Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.200C>T
  hgvsp: ENSP00000428685.1:p.His68Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.358C>T
  hgvsp: ENSP00000346119.4:p.His120Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.958C>T
  hgvsp: ENSP00000429064.1:p.His320Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4788G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.193C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.970C>T
  hgvsp: ENSP00000322804.5:p.His324Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.958C>T
  hgvsp: ENSP00000367256.3:p.His320Tyr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.500C>T
  hgvsp: ENSP00000428348.1:p.His168Tyr
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His320Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

8-125575104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575104
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575104
    reference: chr 8
allele count: 1
allele frequency: 8.316284949187499e-6
allele num: 120246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.189C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.954C>T
  hgvsp: ENST00000378017.3:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.624C>T
  hgvsp: ENST00000524090.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.954C>T
  hgvsp: ENST00000518547.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.496C>T
  hgvsp: ENST00000523179.1:c.496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.354C>T
  hgvsp: ENST00000431961.2:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.227C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.966C>T
  hgvsp: ENST00000325064.5:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.354C>T
  hgvsp: ENST00000522118.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.156C>T
  hgvsp: ENST00000395508.2:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.354C>T
  hgvsp: ENST00000354184.4:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.196C>T
  hgvsp: ENST00000519168.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4784G>A
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29680
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser318Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

8-125575109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575109
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575109
    reference: chr 8
allele count: 1
allele frequency: 8.322929671244279e-6
allele num: 120150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4779C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.222G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.349G>A
  hgvsp: ENSP00000428145.1:p.Val117Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.349G>A
  hgvsp: ENSP00000346119.4:p.Val117Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.949G>A
  hgvsp: ENSP00000367256.3:p.Val317Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.949G>A
  hgvsp: ENSP00000429064.1:p.Val317Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.151G>A
  hgvsp: ENSP00000378884.2:p.Val51Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.491G>A
  hgvsp: ENSP00000428348.1:p.Val165Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.184G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.349G>A
  hgvsp: ENSP00000393606.2:p.Val117Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.961G>A
  hgvsp: ENSP00000322804.5:p.Val321Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.619G>A
  hgvsp: ENSP00000428319.1:p.Val207Met
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.191G>A
  hgvsp: ENSP00000428685.1:p.Val65Met
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29601
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val317Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-125575110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575110
    reference: chr 8
allele count: 26
allele frequency: 2.163961714523512e-4
allele num: 120150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.150C>T
  hgvsp: ENST00000395508.2:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4778G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.948C>T
  hgvsp: ENST00000518547.1:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.348C>T
  hgvsp: ENST00000431961.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.490C>T
  hgvsp: ENST00000523179.1:c.490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.221C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.190C>T
  hgvsp: ENST00000519168.1:c.190C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.960C>T
  hgvsp: ENST00000325064.5:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.618C>T
  hgvsp: ENST00000524090.1:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.183C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.348C>T
  hgvsp: ENST00000522118.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.948C>T
  hgvsp: ENST00000378017.3:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.348C>T
  hgvsp: ENST00000354184.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ser316Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

8-125575112-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575112
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575112
    reference: chr 8
allele count: 1
allele frequency: 8.329030001166064e-6
allele num: 120062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.219A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.346A>G
  hgvsp: ENSP00000346119.4:p.Ser116Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4776T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.346A>G
  hgvsp: ENSP00000428145.1:p.Ser116Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.946A>G
  hgvsp: ENSP00000367256.3:p.Ser316Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.946A>G
  hgvsp: ENSP00000429064.1:p.Ser316Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.958A>G
  hgvsp: ENSP00000322804.5:p.Ser320Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.188A>G
  hgvsp: ENSP00000428685.1:p.Ser64Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.488A>G
  hgvsp: ENSP00000428348.1:p.Ser164Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.616A>G
  hgvsp: ENSP00000428319.1:p.Ser206Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.346A>G
  hgvsp: ENSP00000393606.2:p.Ser116Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.148A>G
  hgvsp: ENSP00000378884.2:p.Ser50Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.181A>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser316Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-125575130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575130
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575130
    reference: chr 8
allele count: 1
allele frequency: 8.416799932665601e-6
allele num: 118810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4758C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.598G>A
  hgvsp: ENSP00000428319.1:p.Ala200Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.170G>A
  hgvsp: ENSP00000428685.1:p.Ala58Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.328G>A
  hgvsp: ENSP00000393606.2:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.470G>A
  hgvsp: ENSP00000428348.1:p.Ala158Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.928G>A
  hgvsp: ENSP00000367256.3:p.Ala310Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.328G>A
  hgvsp: ENSP00000346119.4:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.928G>A
  hgvsp: ENSP00000429064.1:p.Ala310Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.328G>A
  hgvsp: ENSP00000428145.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.130G>A
  hgvsp: ENSP00000378884.2:p.Ala44Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.940G>A
  hgvsp: ENSP00000322804.5:p.Ala314Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.163G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.201G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala310Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

8-125575143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575143
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575143
    reference: chr 8
allele count: 1
allele frequency: 8.528202766548977e-6
allele num: 117258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4745G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.915C>T
  hgvsp: ENST00000378017.3:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.457C>T
  hgvsp: ENST00000523179.1:c.457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.150C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.188C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.315C>T
  hgvsp: ENST00000522118.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.585C>T
  hgvsp: ENST00000524090.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.157C>T
  hgvsp: ENST00000519168.1:c.157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.915C>T
  hgvsp: ENST00000518547.1:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.117C>T
  hgvsp: ENST00000395508.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.315C>T
  hgvsp: ENST00000431961.2:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.927C>T
  hgvsp: ENST00000325064.5:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.315C>T
  hgvsp: ENST00000354184.4:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn305Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

8-125575144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575144
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575144
    reference: chr 8
allele count: 1
allele frequency: 8.545547769612032e-6
allele num: 117020
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.456A>G
  hgvsp: ENSP00000428348.1:p.Asn153Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.584A>G
  hgvsp: ENSP00000428319.1:p.Asn195Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.314A>G
  hgvsp: ENSP00000346119.4:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.914A>G
  hgvsp: ENSP00000367256.3:p.Asn305Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.149A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.926A>G
  hgvsp: ENSP00000322804.5:p.Asn309Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.914A>G
  hgvsp: ENSP00000429064.1:p.Asn305Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.314A>G
  hgvsp: ENSP00000428145.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.314A>G
  hgvsp: ENSP00000393606.2:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.156A>G
  hgvsp: ENSP00000428685.1:p.Asn53Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.187A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.116A>G
  hgvsp: ENSP00000378884.2:p.Asn39Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4744T>C
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn305Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

8-125575144-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575144
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575144
    reference: chr 8
allele count: 1
allele frequency: 8.545547769612032e-6
allele num: 117020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.926A>C
  hgvsp: ENSP00000322804.5:p.Asn309Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4744T>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.456A>C
  hgvsp: ENSP00000428348.1:p.Asn153Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.116A>C
  hgvsp: ENSP00000378884.2:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.314A>C
  hgvsp: ENSP00000393606.2:p.Asn105Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.914A>C
  hgvsp: ENSP00000429064.1:p.Asn305Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.314A>C
  hgvsp: ENSP00000428145.1:p.Asn105Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.914A>C
  hgvsp: ENSP00000367256.3:p.Asn305Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.156A>C
  hgvsp: ENSP00000428685.1:p.Asn53Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.149A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.187A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.584A>C
  hgvsp: ENSP00000428319.1:p.Asn195Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.314A>C
  hgvsp: ENSP00000346119.4:p.Asn105Thr
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn305Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-125575153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575153
    reference: chr 8
allele count: 4
allele frequency: 3.483106931382794e-5
allele num: 114840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.305G>A
  hgvsp: ENSP00000346119.4:p.Arg102His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.447G>A
  hgvsp: ENSP00000428348.1:p.Arg150His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.305G>A
  hgvsp: ENSP00000393606.2:p.Arg102His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.140G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4735C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.305G>A
  hgvsp: ENSP00000428145.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.107G>A
  hgvsp: ENSP00000378884.2:p.Arg36His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.905G>A
  hgvsp: ENSP00000429064.1:p.Arg302His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.917G>A
  hgvsp: ENSP00000322804.5:p.Arg306His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.178G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.905G>A
  hgvsp: ENSP00000367256.3:p.Arg302His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.147G>A
  hgvsp: ENSP00000428685.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.575G>A
  hgvsp: ENSP00000428319.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25124
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18676
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg302His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-125575154-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575154
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575154
    reference: chr 8
allele count: 5
allele frequency: 4.356007805965988e-5
allele num: 114784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.904C>T
  hgvsp: ENSP00000367256.3:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.106C>T
  hgvsp: ENSP00000378884.2:p.Arg36Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.574C>T
  hgvsp: ENSP00000428319.1:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.304C>T
  hgvsp: ENSP00000393606.2:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.304C>T
  hgvsp: ENSP00000346119.4:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.177C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.446C>T
  hgvsp: ENSP00000428348.1:p.Arg150Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.146C>T
  hgvsp: ENSP00000428685.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.904C>T
  hgvsp: ENSP00000429064.1:p.Arg302Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.304C>T
  hgvsp: ENSP00000428145.1:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4734G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.916C>T
  hgvsp: ENSP00000322804.5:p.Arg306Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.139C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25068
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18895
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg302Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

8-125575159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575159
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575159
    reference: chr 8
allele count: 2
allele frequency: 1.759541111678075e-5
allele num: 113666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.441G>A
  hgvsp: ENSP00000428348.1:p.Arg148His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.299G>A
  hgvsp: ENSP00000393606.2:p.Arg100His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.101G>A
  hgvsp: ENSP00000378884.2:p.Arg34His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.569G>A
  hgvsp: ENSP00000428319.1:p.Arg190His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.141G>A
  hgvsp: ENSP00000428685.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.172G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.299G>A
  hgvsp: ENSP00000346119.4:p.Arg100His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.299G>A
  hgvsp: ENSP00000428145.1:p.Arg100His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.899G>A
  hgvsp: ENSP00000367256.3:p.Arg300His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.911G>A
  hgvsp: ENSP00000322804.5:p.Arg304His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.899G>A
  hgvsp: ENSP00000429064.1:p.Arg300His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4729C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.134G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24034
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg300His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-125575160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575160
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575160
    reference: chr 8
allele count: 10
allele frequency: 8.832361773538245e-5
allele num: 113220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.898C>T
  hgvsp: ENSP00000367256.3:p.Arg300Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.898C>T
  hgvsp: ENSP00000429064.1:p.Arg300Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.298C>T
  hgvsp: ENSP00000346119.4:p.Arg100Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.910C>T
  hgvsp: ENSP00000322804.5:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4728G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.133C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.140C>T
  hgvsp: ENSP00000428685.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.298C>T
  hgvsp: ENSP00000428145.1:p.Arg100Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.440C>T
  hgvsp: ENSP00000428348.1:p.Arg148Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.568C>T
  hgvsp: ENSP00000428319.1:p.Arg190Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.100C>T
  hgvsp: ENSP00000378884.2:p.Arg34Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.171C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.298C>T
  hgvsp: ENSP00000393606.2:p.Arg100Cys
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23677
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg300Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125575165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575165
    reference: chr 8
allele count: 1
allele frequency: 8.905195290932729e-6
allele num: 112294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.893A>G
  hgvsp: ENSP00000429064.1:p.His298Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.293A>G
  hgvsp: ENSP00000393606.2:p.His98Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.128A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4723T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.293A>G
  hgvsp: ENSP00000428145.1:p.His98Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.435A>G
  hgvsp: ENSP00000428348.1:p.His146Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.893A>G
  hgvsp: ENSP00000367256.3:p.His298Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.563A>G
  hgvsp: ENSP00000428319.1:p.His188Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.135A>G
  hgvsp: ENSP00000428685.1:p.His46Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.95A>G
  hgvsp: ENSP00000378884.2:p.His32Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.166A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.905A>G
  hgvsp: ENSP00000322804.5:p.His302Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.293A>G
  hgvsp: ENSP00000346119.4:p.His98Arg
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23036
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His298Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

8-125575173-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575173
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575173
    reference: chr 8
allele count: 1
allele frequency: 9.176669236134053e-6
allele num: 108972
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.885C>G
  hgvsp: ENST00000518547.1:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.285C>G
  hgvsp: ENST00000431961.2:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4715G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.555C>G
  hgvsp: ENST00000524090.1:c.555C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.897C>G
  hgvsp: ENST00000325064.5:c.897C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.285C>G
  hgvsp: ENST00000354184.4:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.285C>G
  hgvsp: ENST00000522118.1:c.285C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.127C>G
  hgvsp: ENST00000519168.1:c.127C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.427C>G
  hgvsp: ENST00000523179.1:c.427C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.885C>G
  hgvsp: ENST00000378017.3:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.87C>G
  hgvsp: ENST00000395508.2:c.87C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.158C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.120C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18025
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro295Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-125575182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575182
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575182
    reference: chr 8
allele count: 8
allele frequency: 7.649353629618297e-5
allele num: 104584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.276G>A
  hgvsp: ENST00000354184.4:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.276G>A
  hgvsp: ENST00000522118.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.276G>A
  hgvsp: ENST00000431961.2:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.149G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.78G>A
  hgvsp: ENST00000395508.2:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.118G>A
  hgvsp: ENST00000519168.1:c.118G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.876G>A
  hgvsp: ENST00000518547.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.546G>A
  hgvsp: ENST00000524090.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.418G>A
  hgvsp: ENST00000523179.1:c.418G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.876G>A
  hgvsp: ENST00000378017.3:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.888G>A
  hgvsp: ENST00000325064.5:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4706C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.111G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8237
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17356
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser292Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

8-125575183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575183
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575183
    reference: chr 8
allele count: 1
allele frequency: 9.557305604404006e-6
allele num: 104632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.148C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.77C>T
  hgvsp: ENSP00000378884.2:p.Ser26Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.875C>T
  hgvsp: ENSP00000429064.1:p.Ser292Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.875C>T
  hgvsp: ENSP00000367256.3:p.Ser292Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.545C>T
  hgvsp: ENSP00000428319.1:p.Ser182Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.887C>T
  hgvsp: ENSP00000322804.5:p.Ser296Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.275C>T
  hgvsp: ENSP00000428145.1:p.Ser92Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.275C>T
  hgvsp: ENSP00000346119.4:p.Ser92Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.275C>T
  hgvsp: ENSP00000393606.2:p.Ser92Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.417C>T
  hgvsp: ENSP00000428348.1:p.Ser140Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.110C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4705G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.117C>T
  hgvsp: ENSP00000428685.1:p.Ser40Leu
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser292Leu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-125575186-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575186
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575186
    reference: chr 8
allele count: 1
allele frequency: 9.84697796246332e-6
allele num: 101554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.414A>G
  hgvsp: ENSP00000428348.1:p.His139Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4702T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.74A>G
  hgvsp: ENSP00000378884.2:p.His25Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.272A>G
  hgvsp: ENSP00000346119.4:p.His91Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.872A>G
  hgvsp: ENSP00000367256.3:p.His291Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.145A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.272A>G
  hgvsp: ENSP00000393606.2:p.His91Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.114A>G
  hgvsp: ENSP00000428685.1:p.His39Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.272A>G
  hgvsp: ENSP00000428145.1:p.His91Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.542A>G
  hgvsp: ENSP00000428319.1:p.His181Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.107A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.884A>G
  hgvsp: ENSP00000322804.5:p.His295Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.872A>G
  hgvsp: ENSP00000429064.1:p.His291Arg
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His291Arg
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

8-125575193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575193
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575193
    reference: chr 8
allele count: 9
allele frequency: 9.049773755656108e-5
allele num: 99450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.265G>A
  hgvsp: ENSP00000346119.4:p.Gly89Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.407G>A
  hgvsp: ENSP00000428348.1:p.Gly137Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4695C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.67G>A
  hgvsp: ENSP00000378884.2:p.Gly23Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.265G>A
  hgvsp: ENSP00000428145.1:p.Gly89Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.107G>A
  hgvsp: ENSP00000428685.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.138G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.265G>A
  hgvsp: ENSP00000393606.2:p.Gly89Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.535G>A
  hgvsp: ENSP00000428319.1:p.Gly179Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.865G>A
  hgvsp: ENSP00000429064.1:p.Gly289Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.100G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.865G>A
  hgvsp: ENSP00000367256.3:p.Gly289Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.877G>A
  hgvsp: ENSP00000322804.5:p.Gly293Ser
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15730
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly289Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

8-125575194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575194
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575194
    reference: chr 8
allele count: 3
allele frequency: 3.059289021231466e-5
allele num: 98062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.876C>T
  hgvsp: ENST00000325064.5:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4694G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.406C>T
  hgvsp: ENST00000523179.1:c.406C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.264C>T
  hgvsp: ENST00000354184.4:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.534C>T
  hgvsp: ENST00000524090.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.864C>T
  hgvsp: ENST00000518547.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.66C>T
  hgvsp: ENST00000395508.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.106C>T
  hgvsp: ENST00000519168.1:c.106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.264C>T
  hgvsp: ENST00000522118.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.264C>T
  hgvsp: ENST00000431961.2:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.137C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.864C>T
  hgvsp: ENST00000378017.3:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.99C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser288Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-125575197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125575197
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125575197
    reference: chr 8
allele count: 1
allele frequency: 1.029251322587949e-5
allele num: 97158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.261C>T
  hgvsp: ENST00000431961.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.134C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.96C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.261C>T
  hgvsp: ENST00000522118.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.861C>T
  hgvsp: ENST00000378017.3:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.861C>T
  hgvsp: ENST00000518547.1:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.63C>T
  hgvsp: ENST00000395508.2:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.531C>T
  hgvsp: ENST00000524090.1:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-4691G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.261C>T
  hgvsp: ENST00000354184.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.403C>T
  hgvsp: ENST00000523179.1:c.403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.873C>T
  hgvsp: ENST00000325064.5:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.103C>T
  hgvsp: ENST00000519168.1:c.103C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser287Ser
num of homozygotes: 0
population: European (Finnish)
reference allele: G

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

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 486
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34504
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6790
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10807
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.314060446780552e-4
allele num: 7610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.554e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQ
type: SiteQuality
SIO_000300: 5.652e1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 8.92e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 5.22208e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

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

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

GenotypeDepth
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10446
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7553
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 4.71253534401508e-4
allele num: 2122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.950495049504951e-4
allele num: 2020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.677e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.058e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.076e0

QD
type: SiteQuality
SIO_000300: 6.76e0

FS
type: SiteQuality
SIO_000300: 1.386e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

DP
type: SiteQuality
SIO_000300: 6.02737e5

GenotypeDepth
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 8
bin: 4.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 949
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7482
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34953
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.357378595002357e-4
allele num: 8484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2200
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.05557e5

FS
type: SiteQuality
SIO_000300: 5.731e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.11e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 974
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34985
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10528
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1341
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.747126436781609e-5
allele num: 17400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.664e0

DP
type: SiteQuality
SIO_000300: 6.12402e5

QD
type: SiteQuality
SIO_000300: 4.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.888e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

GenotypeDepth
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1878
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4955
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7099
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34628
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.232862375719518e-5
allele num: 19110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8788
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.28e-1

QD
type: SiteQuality
SIO_000300: 1.036e1

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

DP
type: SiteQuality
SIO_000300: 6.30737e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

GenotypeDepth
all individuals: 5
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 209
bin: 3.25e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7099
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34628
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.232862375719518e-5
allele num: 19110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.413746017296313e-4
allele num: 8788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

DP
type: SiteQuality
SIO_000300: 6.30737e5

QD
type: SiteQuality
SIO_000300: 1.036e1

FS
type: SiteQuality
SIO_000300: 9.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9273
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1297
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 806
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34723
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7576
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2462
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.20656e5

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

FS
type: SiteQuality
SIO_000300: 1.808e0

QD
type: SiteQuality
SIO_000300: 9.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2058
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1182
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.312367190820229e-5
allele num: 18824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.10946e5

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

QD
type: SiteQuality
SIO_000300: 1.385e1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

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

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6325
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11095
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 5.55808e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.674e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

GenotypeDepth
all individuals: 18
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5123
bin: 2.25e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 329
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 11162
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2422
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5583
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1232
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3962
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 453
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 27669
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1027
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 5.88235294117647e-4
allele num: 1700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.897503103876396e-5
allele num: 14498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.605381165919282e-4
allele num: 1784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.035502958579882e-2
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.065040650406504e-3
allele num: 246
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.307e0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

FS
type: SiteQuality
SIO_000300: 2.51646e2

DP
type: SiteQuality
SIO_000300: 5.44301e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.239e0

VQSLOD
type: SiteQuality
SIO_000300: -2.895e2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

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

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1670
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12161
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30701
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1966
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.517205422314912e-5
allele num: 15344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.3426e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.684e1

VQSLOD
type: SiteQuality
SIO_000300: -1.457e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.73e-1

GenotypeDepth
all individuals: 1647
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 872
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5884
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1099
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31399
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12460
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.60414740457007e-5
allele num: 15142
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 2.105263157894737e-3
allele num: 1900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1142
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.66e-2

DP
type: SiteQuality
SIO_000300: 5.31861e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 7.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.235e1

FS
type: SiteQuality
SIO_000300: 9.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31401
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13141
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5630
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.2167e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.77e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.263e0

QD
type: SiteQuality
SIO_000300: 2.402e1

GenotypeDepth
all individuals: 4185
bin: 2.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14437
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28562
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.089e0

QD
type: SiteQuality
SIO_000300: 3.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.61e-1

DP
type: SiteQuality
SIO_000300: 5.03597e5

GenotypeDepth
all individuals: 204
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17373
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25820
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.424599831508003e-5
allele num: 11870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 6.69e0

DP
type: SiteQuality
SIO_000300: 4.70117e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.08e-2

QD
type: SiteQuality
SIO_000300: 6.74e0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 905
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19339
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3646
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.936507936507937e-4
allele num: 1260
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11012
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

QD
type: SiteQuality
SIO_000300: 8.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 4.50891e5

MQ
type: SiteQuality
SIO_000300: 5.714e1

FS
type: SiteQuality
SIO_000300: 3.213e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.91e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.557e-1

GenotypeDepth
all individuals: 26570
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1096
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6685
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 995
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2626
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19964
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26167
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3444
bin: 6.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.269e0

VQSLOD
type: SiteQuality
SIO_000300: -1.725e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

DP
type: SiteQuality
SIO_000300: 4.43401e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeDepth
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21343
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1056
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7274
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.25e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -1.823e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 8.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.31577e5

GenotypeDepth
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 122
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23979
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 940
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.409244644870349e-4
allele num: 7096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 938
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 4.06188e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.628e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.72e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.383e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.93e0

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

GenotypeDepth
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2962
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2581
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14549
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1966
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29525
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.484119916889285e-4
allele num: 6738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 3.46023e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 8.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -1.941e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

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

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

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2935
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29639
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14788
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1644
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.4584e5

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 7.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.91e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.471e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeDepth
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29700
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 920
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14981
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.45033e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.89e-2

QD
type: SiteQuality
SIO_000300: 3.78e0

VQSLOD
type: SiteQuality
SIO_000300: -2.26e0

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

GenotypeDepth
all individuals: 4925
bin: 1.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 14409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29873
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572821642025794e-4
allele num: 6358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.41752e5

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.03e-2

QD
type: SiteQuality
SIO_000300: 1.089e1

VQSLOD
type: SiteQuality
SIO_000300: -1.215e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30215
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 3.385e5

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 7.77e0

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

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

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

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9602
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31223
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3626
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.591343093570974e-4
allele num: 6284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.286e0

QD
type: SiteQuality
SIO_000300: 1.53e1

DP
type: SiteQuality
SIO_000300: 3.08935e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.559e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.850000000000001e-2

GenotypeDepth
all individuals: 102
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 874
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3830
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31238
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4838
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 5.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.94e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -2.572e0

DP
type: SiteQuality
SIO_000300: 3.02483e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

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

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

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

GenotypeQuality
all individuals: 30771
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6847
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5099
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4544
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2637
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

FS
type: SiteQuality
SIO_000300: 3.042e0

VQSLOD
type: SiteQuality
SIO_000300: -1.796e0

DP
type: SiteQuality
SIO_000300: 2.91052e5

GenotypeDepth
all individuals: 262
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2321
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1486
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5031
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 604
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7442
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65732
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15944
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738525730180807e-4
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 3.439465408805032e-3
allele num: 10176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

DP
type: SiteQuality
SIO_000300: 1.630758e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.302e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5002
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1320
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5639870991298e-5
allele num: 65732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 3.633e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.423e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.63169e6

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7460
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.250781347668459e-5
allele num: 15998
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.633514e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.197e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.849e0

GenotypeDepth
all individuals: 351
bin: 8.75e1
variant carriers: 343

GenotypeDepth
all individuals: 502
bin: 7.75e1
variant carriers: 489

GenotypeDepth
all individuals: 292
bin: 9.25e1
variant carriers: 281

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 36468
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 287
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 291
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7198
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1886
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1680
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 9908
bin: 9.75e1
variant carriers: 8625

GenotypeQuality
all individuals: 379
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 271
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 7

Other
type: Population
allele count: 67
allele frequency: 7.562076749435666e-2
allele num: 886
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 735
allele frequency: 1.13566131025958e-1
allele num: 6472
num of homozygotes: 38

European (Non-Finnish)
type: Population
allele count: 5070
allele frequency: 7.6646308278406e-2
allele num: 66148
num of homozygotes: 209

South Asian
type: Population
allele count: 1138
allele frequency: 6.933950767730929e-2
allele num: 16412
num of homozygotes: 45

East Asian
type: Population
allele count: 1453
allele frequency: 1.686788948223822e-1
allele num: 8614
num of homozygotes: 118

Latino
type: Population
allele count: 311
allele frequency: 2.69357353195912e-2
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 352
allele frequency: 3.434146341463415e-2
allele num: 10250
num of homozygotes: 8

QD
type: SiteQuality
SIO_000300: 1.389e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.89e-2

DP
type: SiteQuality
SIO_000300: 1.896427e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

VQSLOD
type: SiteQuality
SIO_000300: 6.85e0

GenotypeDepth
all individuals: 1396
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8320
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2050
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.761811792268645e-5
allele num: 10244
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

DP
type: SiteQuality
SIO_000300: 1.611589e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

FS
type: SiteQuality
SIO_000300: 2.828e0

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

GenotypeDepth
all individuals: 46
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 76
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 198
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8653
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 42923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66276
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.748488984207447e-5
allele num: 10258
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.246026931942254e-4
allele num: 16486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 5.962e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.24e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

DP
type: SiteQuality
SIO_000300: 1.616385e6

GenotypeDepth
all individuals: 8385
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 76
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 603
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8668
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43066
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
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: 8644
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.75609756097561e-5
allele num: 10250
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.617704e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.046e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 599
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29190
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43552
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2037
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.654e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.62349e6

FS
type: SiteQuality
SIO_000300: 3.506e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.925e0

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeDepth
all individuals: 123
bin: 5.75e1
variant carriers: 7

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

GenotypeDepth
all individuals: 78
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 48
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 17
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 20
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 43648
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 2283
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 6.020832078993316e-4
allele num: 66436
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.712509712509713e-5
allele num: 10296
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.55e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

DP
type: SiteQuality
SIO_000300: 1.626423e6

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

GenotypeDepth
all individuals: 68
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 350
bin: 4.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 29221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 43648
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2283
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8707
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

VQSLOD
type: SiteQuality
SIO_000300: 5.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 1.626423e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29297
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8426
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19344
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8739
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2033
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513721714010592e-5
allele num: 66464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.815e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.625283e6

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeDepth
all individuals: 132
bin: 1.75e1
variant carriers: 11

GenotypeDepth
all individuals: 362
bin: 9.75e1
variant carriers: 332

GenotypeDepth
all individuals: 101
bin: 8.75e1
variant carriers: 92

GenotypeDepth
all individuals: 158
bin: 6.75e1
variant carriers: 118

GenotypeDepth
all individuals: 109
bin: 7.75e1
variant carriers: 96

GenotypeDepth
all individuals: 8215
bin: 3.25e1
variant carriers: 89

GenotypeQuality
all individuals: 1899
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 755
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8578
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 299
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43470
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2706
bin: 9.75e1
variant carriers: 1849

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 5

Latino
type: Population
allele count: 148
allele frequency: 1.280055353745027e-2
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.8125e-3
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.539882968894364e-4
allele num: 6494
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 137
allele frequency: 2.05922140387795e-3
allele num: 66530
num of homozygotes: 0

African
type: Population
allele count: 1725
allele frequency: 1.666344667697063e-1
allele num: 10352
num of homozygotes: 144

South Asian
type: Population
allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.229e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

DP
type: SiteQuality
SIO_000300: 1.690908e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.037e0

QD
type: SiteQuality
SIO_000300: 1.307e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.69e0

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1219
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8488
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.434e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

DP
type: SiteQuality
SIO_000300: 1.617054e6

GenotypeDepth
all individuals: 155
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44804
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8902
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 776
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.096229470275272e-4
allele num: 8646
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.617869e6

FS
type: SiteQuality
SIO_000300: 1.755e0

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

QD
type: SiteQuality
SIO_000300: 9.31e0

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

GenotypeDepth
all individuals: 8495
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 939
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8913
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.12e1

DP
type: SiteQuality
SIO_000300: 1.617994e6

MQ
type: SiteQuality
SIO_000300: 5.892e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30004
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 771
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44848
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8925
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.335e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.911e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.61847e6

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44851
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 768
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
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: 896
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.54e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.22e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.685e0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e-1

DP
type: SiteQuality
SIO_000300: 1.618261e6

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1216
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.616432e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: 8.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.23e1

FS
type: SiteQuality
SIO_000300: 2.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1211
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e0

QD
type: SiteQuality
SIO_000300: 1.017e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.151e0

VQSLOD
type: SiteQuality
SIO_000300: -5.926e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.552e0

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

DP
type: SiteQuality
SIO_000300: 1.608173e6

GenotypeDepth
all individuals: 18488
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 735
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42909
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.696e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

DP
type: SiteQuality
SIO_000300: 1.601971e6

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

FS
type: SiteQuality
SIO_000300: 3.208e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.555e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1903
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8497
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

FS
type: SiteQuality
SIO_000300: 1.606e0

VQSLOD
type: SiteQuality
SIO_000300: -2.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.59816e6

QD
type: SiteQuality
SIO_000300: 2.139e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

GenotypeDepth
all individuals: 40
bin: 9.75e1
variant carriers: 9

GenotypeDepth
all individuals: 601
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 29597
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43482
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.460387002555677e-3
allele num: 16434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.161e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.598945e6

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeDepth
all individuals: 1135
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29591
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508887346470713e-5
allele num: 66274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 7.156e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.881e0

DP
type: SiteQuality
SIO_000300: 1.595078e6

MQRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

GenotypeDepth
all individuals: 1522
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 889
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.827683615819209e-5
allele num: 11328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5898
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.565215e6

QD
type: SiteQuality
SIO_000300: 2.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 9.118e0

VQSLOD
type: SiteQuality
SIO_000300: -3.225e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41180
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53666482266888e-5
allele num: 65076
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.849e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.003e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.474e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
type: SiteQuality
SIO_000300: 1.52847e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539029795616843e-5
allele num: 64976
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

DP
type: SiteQuality
SIO_000300: 1.522864e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7384
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3917
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539029795616843e-5
allele num: 64976
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 1.522864e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.385e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

GenotypeDepth
all individuals: 3067
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2159
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1549
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15852
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.848428835489834e-4
allele num: 10820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564308731971342e-5
allele num: 63926
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.212121212121212e-4
allele num: 8250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.392e0

MQ
type: SiteQuality
SIO_000300: 5.898e1

QD
type: SiteQuality
SIO_000300: 1.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

DP
type: SiteQuality
SIO_000300: 1.472338e6

GenotypeDepth
all individuals: 3703
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 437
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5756
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565239168544954e-5
allele num: 63888
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.109452736318408e-4
allele num: 9648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10808
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.313131313131313e-5
allele num: 15840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

QD
type: SiteQuality
SIO_000300: 2.102e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

DP
type: SiteQuality
SIO_000300: 1.470568e6

FS
type: SiteQuality
SIO_000300: 4.957e0

VQSLOD
type: SiteQuality
SIO_000300: -1.786e0

GenotypeDepth
all individuals: 2226
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4254
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63352
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.04777870913663e-4
allele num: 9544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10664
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.847745750184775e-4
allele num: 5412
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e0

QD
type: SiteQuality
SIO_000300: 1.042e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

FS
type: SiteQuality
SIO_000300: 1.562e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.445441e6

GenotypeDepth
all individuals: 4444
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 194
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5420
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7004
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36852
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1089
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.858736059479554e-4
allele num: 5380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15658
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.695491500369549e-4
allele num: 8118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.442870632672332e-5
allele num: 10590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.916152116779076e-5
allele num: 63162
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 2.144e1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 1.436224e6

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5934
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7834
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 454
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5252
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.06224771616741e-4
allele num: 9414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62762
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.56e0

QD
type: SiteQuality
SIO_000300: 9.98e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.415572e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.45e-1

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 640
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33875
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.636393388970709e-5
allele num: 61110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.738e1

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.35935e6

FS
type: SiteQuality
SIO_000300: 8.414999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -2.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18627
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1312
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 13369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4472
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1800
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.137138958380714e-4
allele num: 8794
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.321979776476849e-4
allele num: 7516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.103429504627109e-5
allele num: 58784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14794
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2464e1

VQSLOD
type: SiteQuality
SIO_000300: -1.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.3e-2

DP
type: SiteQuality
SIO_000300: 1.286915e6

GenotypeDepth
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17528
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30912
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13567
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699813020567737e-5
allele num: 58830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.87e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 8.82e0

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.117e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.283716e6

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 15422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.910850034554251e-5
allele num: 14470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7308
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.04e-1

FS
type: SiteQuality
SIO_000300: 9.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.24e-1

DP
type: SiteQuality
SIO_000300: 1.238841e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.058e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

GenotypeDepth
all individuals: 2908
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17542
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 9.75e1
variant carriers: 9

South Asian
type: Population
allele count: 1
allele frequency: 7.023458350891979e-5
allele num: 14238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.06547338671691e-4
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.151277918489523e-4
allele num: 8686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.786416092036157e-5
allele num: 55978
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.067e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.200308e6

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

GenotypeDepth
all individuals: 10844
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2047
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 635
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3421
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.625552896816765e-5
allele num: 55164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14118
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.191327138432213e-4
allele num: 8394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.957e0

QD
type: SiteQuality
SIO_000300: 8.33e0

DP
type: SiteQuality
SIO_000300: 1.18452e6

MQRankSum
type: SiteQuality
SIO_000300: 3.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 16
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2078
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 554
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4096
num of homozygotes: 0