12-57908807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908807
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908807
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.101C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1471C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1468C>T
  hgvsp: ENSP00000314653.5:p.Pro490Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2170C>T
  hgvsp: ENSP00000262027.5:p.Pro724Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*462C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.677C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1671C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro724Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

12-57908816-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908816
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908816
    reference: chr 12
allele count: 6
allele frequency: 4.94266508501384e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*471C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.110C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2179C>T
  hgvsp: ENSP00000262027.5:p.Arg727Trp
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1680C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1477C>T
  hgvsp: ENSP00000314653.5:p.Arg493Trp
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.686C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1462C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+19C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3473
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7435
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg727Trp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-57908817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908817
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908817
    reference: chr 12
allele count: 611
allele frequency: 5.033280611572427e-3
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1681G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1461G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.111G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.687G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+20G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1478G>A
  hgvsp: ENSP00000314653.5:p.Arg493Gln
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2180G>A
  hgvsp: ENSP00000262027.5:p.Arg727Gln
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*472G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22719
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 9730
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 8.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 6.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 5.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 5.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg727Gln
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

12-57908841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908841
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908841
    reference: chr 12
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204G>A
  hgvsp: ENSP00000262027.5:p.Arg735Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1437G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+44G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502G>A
  hgvsp: ENSP00000314653.5:p.Arg501Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg735Lys
num of homozygotes: 1
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/12-57908844-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908844
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908844
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+3A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+47A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+3A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+3A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1434A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+3A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+3A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+3A>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 8.75e1
  variant carriers: 0
hgvs: c.2204+3A>C
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

12-57908849-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908849
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908849
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+8A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+8A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+8A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+8A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+8A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1429A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+52A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+8A>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6939
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7554
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2204+8A>G
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-57908850-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908850
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908850
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+9G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+53G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+9G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+9G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+9G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+9G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1428G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+9G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2845
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6937
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

12-57908851-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908851
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908851
    reference: chr 12
allele count: 13
allele frequency: 1.071193144363876e-4
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1427C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+10C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+54C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6932
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3427
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33470
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-57908852-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908852
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908852
    reference: chr 12
allele count: 257
allele frequency: 2.11784095591265e-3
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1426G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+11G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+55G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 5.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 4.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 22898
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 2
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/12-57908856-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908856
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908856
    reference: chr 12
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+15A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+15A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+15A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+15A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+59A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+15A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1422A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+15A>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2847
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6746
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

12-57908864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908864
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908864
    reference: chr 12
allele count: 96
allele frequency: 7.910219014188955e-4
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1414C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+23C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+67C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 22985
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff

12-57908874-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908874
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908874
    reference: chr 12
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+77A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+33A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1404A>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

12-57908881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908881
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908881
    reference: chr 12
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+40C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+40C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+40C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+40C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+40C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+84C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1397C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+40C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

12-57908884-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908884
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908884
    reference: chr 12
allele count: 1144
allele frequency: 1.144480681886392e-2
allele num: 99958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1394G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+43G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+87G>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9346
  bin: 3.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 4.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 5.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 4.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 23570
  bin: 2.75e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 2.75e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 5.25e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 8400
  bin: 2.5e0
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 6.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 1.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 64
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

12-57908886-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908886
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908886
    reference: chr 12
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+89A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+45A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1392A>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31649
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

12-57908886-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908886
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908886
    reference: chr 12
allele count: 74
allele frequency: 6.117118010779353e-4
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+89A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1392A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.135+45A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1502+45A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.711+45A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1705+45A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2204+45A>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*496+45A>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9676
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31649
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43199
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 8.25e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

12-57908888-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908888
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908888
    reference: chr 12
allele count: 8
allele frequency: 6.597285217133149e-5
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+91G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-45G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1390G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31877
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

12-57908890-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908890
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908890
    reference: chr 12
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-43T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-43T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-43T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-43T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-43T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1388T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+93T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-43T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

12-57908894-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908894
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908894
    reference: chr 12
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1384T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-39T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+97T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-57908897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908897
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908897
    reference: chr 12
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-36T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1381T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-36T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.228+100T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-36T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-36T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-36T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-36T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

12-57908899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908899
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908899
    reference: chr 12
allele count: 3
allele frequency: 2.473003050037095e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1379C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-34C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-101C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32207
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

12-57908906-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908906
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908906
    reference: chr 12
allele count: 12
allele frequency: 9.943487844086111e-5
allele num: 120682
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-27T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1372T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-27T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-27T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-27T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-94T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-27T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-27T>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13858
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

12-57908910-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908910
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908910
    reference: chr 12
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1368G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-23G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-90G>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

12-57908918-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908918
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908915
    reference: chr 12
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2205-11_2205-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.712-11_712-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.136-11_136-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1356_134-1354delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*497-11_*497-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1503-11_1503-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1706-11_*1706-9delCTC
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-78_229-76delCTC
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7583
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45881
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: TCTC
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/12-57908937-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908937
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908937
    reference: chr 12
allele count: 47
allele frequency: 3.872966692486445e-4
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2209C>A
  hgvsp: ENST00000262027.5:c.2209C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.140C>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.716C>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1507C>A
  hgvsp: ENST00000315473.5:c.1507C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.5C>A
  hgvsp: ENST00000547665.1:c.5C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1710C>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*501C>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1341C>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-63C>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg737Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

12-57908937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908937
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908937
    reference: chr 12
allele count: 4
allele frequency: 3.29614186594591e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*501C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.5C>T
  hgvsp: ENSP00000448910.1:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2209C>T
  hgvsp: ENSP00000262027.5:p.Arg737Trp
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-63C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1507C>T
  hgvsp: ENSP00000314653.5:p.Arg503Trp
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.140C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.716C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1710C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1341C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7556
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg737Trp
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

12-57908958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908958
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908958
    reference: chr 12
allele count: 3
allele frequency: 2.495508085446197e-5
allele num: 120216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1528T>C
  hgvsp: ENST00000315473.5:c.1528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*522T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1731T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.26T>C
  hgvsp: ENST00000547665.1:c.26T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-42T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1320T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.737T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2230T>C
  hgvsp: ENST00000262027.5:c.2230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.161T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu744Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

12-57908960-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908960
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908960
    reference: chr 12
allele count: 12
allele frequency: 9.992339206608267e-5
allele num: 120092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.28G>T
  hgvsp: ENSP00000448910.1:p.Leu10Phe
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1530G>T
  hgvsp: ENSP00000314653.5:p.Leu510Phe
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1733G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2232G>T
  hgvsp: ENSP00000262027.5:p.Leu744Phe
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.739G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1318G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.163G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-40G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*524G>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14010
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46126
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu744Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

12-57908964-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908964
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908964
    reference: chr 12
allele count: 6
allele frequency: 4.947392724034434e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.32G>T
  hgvsp: ENSP00000448910.1:p.Val12Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2236G>T
  hgvsp: ENSP00000262027.5:p.Val746Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*528G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.1G>T
  hgvsp: ENSP00000447335.1:p.Val1?
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.743G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1534G>T
  hgvsp: ENSP00000314653.5:p.Val512Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1314G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1737G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-36G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.167G>T
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val1?
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-57908965-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908965
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908965
    reference: chr 12
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1738T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.33T>G
  hgvsp: ENSP00000448910.1:p.Val12Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*529T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2237T>G
  hgvsp: ENSP00000262027.5:p.Val746Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.744T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1313T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.168T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-35T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1535T>G
  hgvsp: ENSP00000314653.5:p.Val512Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.2T>G
  hgvsp: ENSP00000447335.1:p.Val1?
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47082
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val1?
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

12-57908969-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908969
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908969
    reference: chr 12
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1309T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.4T>C
  hgvsp: ENST00000551172.1:c.4T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.6T>C
  hgvsp: ENST00000552499.1:c.6T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.37T>C
  hgvsp: ENST00000547665.1:c.37T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1539T>C
  hgvsp: ENST00000315473.5:c.1539T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1742T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*533T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.172T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2241T>C
  hgvsp: ENST00000262027.5:c.2241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.748T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-31T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn747Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

12-57908970-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908970
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908970
    reference: chr 12
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2242A>G
  hgvsp: ENSP00000262027.5:p.Ile748Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*534A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-30A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1743A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1308A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1540A>G
  hgvsp: ENSP00000314653.5:p.Ile514Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.7A>G
  hgvsp: ENSP00000447335.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.5A>G
  hgvsp: ENSP00000448378.1:p.Ile3Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.173A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.749A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.38A>G
  hgvsp: ENSP00000448910.1:p.Ile14Val
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile748Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

12-57908977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908977
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908977
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.14C>T
  hgvsp: ENSP00000447335.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1301C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*541C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.180C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2249C>T
  hgvsp: ENSP00000262027.5:p.Ala750Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.45C>T
  hgvsp: ENSP00000448910.1:p.Ala16Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1750C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.12C>T
  hgvsp: ENSP00000448378.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.756C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1547C>T
  hgvsp: ENSP00000314653.5:p.Ala516Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-23C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala750Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

12-57908984-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908984
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908984
    reference: chr 12
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1757C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.21C>G
  hgvsp: ENST00000552499.1:c.21C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1294C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2256C>G
  hgvsp: ENST00000262027.5:c.2256C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-16C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.763C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1554C>G
  hgvsp: ENST00000315473.5:c.1554C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.19C>G
  hgvsp: ENST00000551172.1:c.19C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.52C>G
  hgvsp: ENST00000547665.1:c.52C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.187C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*548C>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu752Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

12-57908984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908984
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908984
    reference: chr 12
allele count: 6
allele frequency: 4.94323518265254e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.21C>T
  hgvsp: ENST00000552499.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2256C>T
  hgvsp: ENST00000262027.5:c.2256C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1554C>T
  hgvsp: ENST00000315473.5:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1294C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*548C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.763C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.52C>T
  hgvsp: ENST00000547665.1:c.52C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.19C>T
  hgvsp: ENST00000551172.1:c.19C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.187C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1757C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-16C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu752Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

12-57908986-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908986
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908984
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.25_26delGT
  hgvsp: ENSP00000447335.1:p.Val9HisfsTer10
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1761_*1762delGT
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2260_2261delGT
  hgvsp: ENSP00000262027.5:p.Val754HisfsTer10
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.191_192delGT
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1558_1559delGT
  hgvsp: ENSP00000314653.5:p.Val520HisfsTer10
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1290_134-1289delGT
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.23_24delGT
  hgvsp: ENSP00000448378.1:p.Val9HisfsTer10
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.767_768delGT
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*552_*553delGT
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.56_57delGT
  hgvsp: ENSP00000448910.1:p.Val20HisfsTer10
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-12_229-11delGT
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val754HisfsTer10
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: CTG
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-57908987-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908987
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908987
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.766T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.190T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1291T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2259T>G
  hgvsp: ENST00000262027.5:c.2259T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1760T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1557T>G
  hgvsp: ENST00000315473.5:c.1557T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.24T>G
  hgvsp: ENST00000552499.1:c.24T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.22T>G
  hgvsp: ENST00000551172.1:c.22T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.55T>G
  hgvsp: ENST00000547665.1:c.55T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*551T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-13T>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser753Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

12-57908988-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908988
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908988
    reference: chr 12
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*552G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-12G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1290G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.56G>C
  hgvsp: ENSP00000448910.1:p.Val20Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1558G>C
  hgvsp: ENSP00000314653.5:p.Val520Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.191G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1761G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.23G>C
  hgvsp: ENSP00000448378.1:p.Val9Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.767G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.25G>C
  hgvsp: ENSP00000447335.1:p.Val9Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2260G>C
  hgvsp: ENSP00000262027.5:p.Val754Leu
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val754Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

12-57908992-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908992
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908992
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2264T>C
  hgvsp: ENSP00000262027.5:p.Met755Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-8T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.29T>C
  hgvsp: ENSP00000447335.1:p.Met10Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.27T>C
  hgvsp: ENSP00000448378.1:p.Met10Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.60T>C
  hgvsp: ENSP00000448910.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.771T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1562T>C
  hgvsp: ENSP00000314653.5:p.Met521Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.195T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1286T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1765T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*556T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met755Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-57908996-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57908996
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57908996
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.775T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2268T>G
  hgvsp: ENST00000262027.5:c.2268T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*560T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.31T>G
  hgvsp: ENST00000551172.1:c.31T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.229-4T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1282T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.64T>G
  hgvsp: ENST00000547665.1:c.64T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.33T>G
  hgvsp: ENST00000552499.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1566T>G
  hgvsp: ENST00000315473.5:c.1566T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.199T>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1769T>G
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.229-4T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/12-57909004-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909004
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909004
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.39A>C
  hgvsp: ENSP00000448378.1:p.Tyr14Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*568A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.41A>C
  hgvsp: ENSP00000447335.1:p.Tyr14Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2276A>C
  hgvsp: ENSP00000262027.5:p.Tyr759Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.207A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.72A>C
  hgvsp: ENSP00000448910.1:p.Tyr25Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.233A>C
  hgvsp: ENSP00000449787.1:p.Tyr78Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1574A>C
  hgvsp: ENSP00000314653.5:p.Tyr525Ser
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.783A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1777A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1274A>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr759Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS

12-57909005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909005
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909005
    reference: chr 12
allele count: 3
allele frequency: 2.471821237888076e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.234C>T
  hgvsp: ENST00000552914.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.42C>T
  hgvsp: ENST00000552499.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1273C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1575C>T
  hgvsp: ENST00000315473.5:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.40C>T
  hgvsp: ENST00000551172.1:c.40C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1778C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.73C>T
  hgvsp: ENST00000547665.1:c.73C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.784C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.208C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2277C>T
  hgvsp: ENST00000262027.5:c.2277C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*569C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr759Tyr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

12-57909007-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909007
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909007
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.75T>A
  hgvsp: ENSP00000448910.1:p.Met26Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2279T>A
  hgvsp: ENSP00000262027.5:p.Met760Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*571T>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.42T>A
  hgvsp: ENSP00000448378.1:p.Met15Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.786T>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.236T>A
  hgvsp: ENSP00000449787.1:p.Met79Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1780T>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1577T>A
  hgvsp: ENSP00000314653.5:p.Met526Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.44T>A
  hgvsp: ENSP00000447335.1:p.Met15Lys
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1271T>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.210T>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met760Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

12-57909011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909011
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909011
    reference: chr 12
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*575C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.790C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.79C>T
  hgvsp: ENST00000547665.1:c.79C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2283C>T
  hgvsp: ENST00000262027.5:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.46C>T
  hgvsp: ENST00000551172.1:c.46C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.48C>T
  hgvsp: ENST00000552499.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1784C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1581C>T
  hgvsp: ENST00000315473.5:c.1581C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1267C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.240C>T
  hgvsp: ENST00000552914.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.214C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro761Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

12-57909013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909013
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909013
    reference: chr 12
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1786C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.48C>T
  hgvsp: ENSP00000448378.1:p.Thr17Met
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*577C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.50C>T
  hgvsp: ENSP00000447335.1:p.Thr17Met
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.242C>T
  hgvsp: ENSP00000449787.1:p.Thr81Met
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.792C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2285C>T
  hgvsp: ENSP00000262027.5:p.Thr762Met
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1583C>T
  hgvsp: ENSP00000314653.5:p.Thr528Met
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1265C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.216C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.81C>T
  hgvsp: ENSP00000448910.1:p.Thr28Met
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr762Met
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

12-57909014-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909014
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909014
    reference: chr 12
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.217G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000548202
  gene symbol: MARS
  hgvsc: ENST00000548202.1:n.793G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2286G>T
  hgvsp: ENST00000262027.5:c.2286G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.51G>T
  hgvsp: ENST00000552499.1:c.51G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.243G>T
  hgvsp: ENST00000552914.1:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.82G>T
  hgvsp: ENST00000547665.1:c.82G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1787G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1264G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1584G>T
  hgvsp: ENST00000315473.5:c.1584G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.49G>T
  hgvsp: ENST00000551172.1:c.49G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*578G>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33808
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr762Thr
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: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-57909018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909018
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909018
    reference: chr 12
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.247A>G
  hgvsp: ENSP00000449787.1:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2290A>G
  hgvsp: ENSP00000262027.5:p.Ser764Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1588A>G
  hgvsp: ENSP00000314653.5:p.Ser530Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1791A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1260A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.86A>G
  hgvsp: ENSP00000448910.1:p.Ser30Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*582A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.53A>G
  hgvsp: ENSP00000448378.1:p.Ser19Gly
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.221A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.55A>G
  hgvsp: ENSP00000447335.1:p.Ser19Gly
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser764Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

12-57909021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909021
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909021
    reference: chr 12
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1591G>A
  hgvsp: ENSP00000314653.5:p.Ala531Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.56G>A
  hgvsp: ENSP00000448378.1:p.Ala20Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.58G>A
  hgvsp: ENSP00000447335.1:p.Ala20Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.224G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1257G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1794G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*585G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.250G>A
  hgvsp: ENSP00000449787.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2293G>A
  hgvsp: ENSP00000262027.5:p.Ala765Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.89G>A
  hgvsp: ENSP00000448910.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala765Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

12-57909022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909022
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909022
    reference: chr 12
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*586C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.251C>T
  hgvsp: ENSP00000449787.1:p.Ala84Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1256C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2294C>T
  hgvsp: ENSP00000262027.5:p.Ala765Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.59C>T
  hgvsp: ENSP00000447335.1:p.Ala20Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1592C>T
  hgvsp: ENSP00000314653.5:p.Ala531Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.90C>T
  hgvsp: ENSP00000448910.1:p.Ala31Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.57C>T
  hgvsp: ENSP00000448378.1:p.Ala20Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1795C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.225C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ala765Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

12-57909025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909025
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909025
    reference: chr 12
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1798C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.62C>T
  hgvsp: ENSP00000447335.1:p.Thr21Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.254C>T
  hgvsp: ENSP00000449787.1:p.Thr85Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1595C>T
  hgvsp: ENSP00000314653.5:p.Thr532Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.93C>T
  hgvsp: ENSP00000448910.1:p.Thr32Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.60C>T
  hgvsp: ENSP00000448378.1:p.Thr21Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2297C>T
  hgvsp: ENSP00000262027.5:p.Thr766Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.228C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*589C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1253C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr766Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

12-57909046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909046
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909046
    reference: chr 12
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.249T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1616T>C
  hgvsp: ENSP00000314653.5:p.Leu539Pro
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.275T>C
  hgvsp: ENSP00000449787.1:p.Leu92Pro
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.81T>C
  hgvsp: ENSP00000448378.1:p.Leu28Pro
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1819T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.114T>C
  hgvsp: ENSP00000448910.1:p.Leu39Pro
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2318T>C
  hgvsp: ENSP00000262027.5:p.Leu773Pro
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1232T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*610T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.83T>C
  hgvsp: ENSP00000447335.1:p.Leu28Pro
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu773Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-57909054-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909054
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909054
    reference: chr 12
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1827C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*618C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.283C>G
  hgvsp: ENSP00000449787.1:p.Pro95Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.91C>G
  hgvsp: ENSP00000447335.1:p.Pro31Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2326C>G
  hgvsp: ENSP00000262027.5:p.Pro776Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1624C>G
  hgvsp: ENSP00000314653.5:p.Pro542Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.89C>G
  hgvsp: ENSP00000448378.1:p.Pro31Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.257C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.122C>G
  hgvsp: ENSP00000448910.1:p.Pro42Ala
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1224C>G
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro776Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

12-57909055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909055
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909055
    reference: chr 12
allele count: 2
allele frequency: 1.651527663088357e-5
allele num: 121100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1223C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1625C>T
  hgvsp: ENSP00000314653.5:p.Pro542Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1828C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2327C>T
  hgvsp: ENSP00000262027.5:p.Pro776Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.90C>T
  hgvsp: ENSP00000448378.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*619C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.258C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.284C>T
  hgvsp: ENSP00000449787.1:p.Pro95Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.92C>T
  hgvsp: ENSP00000447335.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.123C>T
  hgvsp: ENSP00000448910.1:p.Pro42Leu
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro776Leu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

12-57909064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909064
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909064
    reference: chr 12
allele count: 1
allele frequency: 8.273625337150233e-6
allele num: 120866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.267G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.293G>A
  hgvsp: ENSP00000449787.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.101G>A
  hgvsp: ENSP00000447335.1:p.Ser34Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1837G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.99G>A
  hgvsp: ENSP00000448378.1:p.Ser34Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1634G>A
  hgvsp: ENSP00000314653.5:p.Ser545Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*628G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.132G>A
  hgvsp: ENSP00000448910.1:p.Ser45Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2336G>A
  hgvsp: ENSP00000262027.5:p.Ser779Asn
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1214G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser779Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-57909076-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909076
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909076
    reference: chr 12
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2348C>T
  hgvsp: ENSP00000262027.5:p.Thr783Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1646C>T
  hgvsp: ENSP00000314653.5:p.Thr549Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*640C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.144C>T
  hgvsp: ENSP00000448910.1:p.Thr49Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1849C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.111C>T
  hgvsp: ENSP00000448378.1:p.Thr38Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.305C>T
  hgvsp: ENSP00000449787.1:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.113C>T
  hgvsp: ENSP00000447335.1:p.Thr38Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.279C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1202C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr783Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

12-57909084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909084
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909084
    reference: chr 12
allele count: 6
allele frequency: 4.994090326447037e-5
allele num: 120142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1857C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.313C>T
  hgvsp: ENST00000552914.1:c.313C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.152C>T
  hgvsp: ENST00000547665.1:c.152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.119C>T
  hgvsp: ENST00000551172.1:c.119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1194C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2356C>T
  hgvsp: ENST00000262027.5:c.2356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.287C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.121C>T
  hgvsp: ENST00000552499.1:c.121C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*648C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1654C>T
  hgvsp: ENST00000315473.5:c.1654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9044
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu786Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

12-57909112-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909112
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909112
    reference: chr 12
allele count: 2
allele frequency: 1.712886041691646e-5
allele num: 116762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1885T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.180T>C
  hgvsp: ENSP00000448910.1:p.Ile61Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.315T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.147T>C
  hgvsp: ENSP00000448378.1:p.Ile50Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1682T>C
  hgvsp: ENSP00000314653.5:p.Ile561Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.341T>C
  hgvsp: ENSP00000449787.1:p.Ile114Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2384T>C
  hgvsp: ENSP00000262027.5:p.Ile795Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.149T>C
  hgvsp: ENSP00000447335.1:p.Ile50Thr
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*676T>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1166T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30110
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile795Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

12-57909115-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909115
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909115
    reference: chr 12
allele count: 1
allele frequency: 8.626043751293907e-6
allele num: 115928
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2387G>T
  hgvsp: ENSP00000262027.5:p.Gly796Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*679G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.183G>T
  hgvsp: ENSP00000448910.1:p.Gly62Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.150G>T
  hgvsp: ENSP00000448378.1:p.Gly51Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1888G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1685G>T
  hgvsp: ENSP00000314653.5:p.Gly562Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.318G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.152G>T
  hgvsp: ENSP00000447335.1:p.Gly51Val
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1163G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.344G>T
  hgvsp: ENSP00000449787.1:p.Gly115Val
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly796Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

12-57909118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909118
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909118
    reference: chr 12
allele count: 11
allele frequency: 9.561060408518036e-5
allele num: 115050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*682C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2390C>T
  hgvsp: ENSP00000262027.5:p.Thr797Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1891C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1688C>T
  hgvsp: ENSP00000314653.5:p.Thr563Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.153C>T
  hgvsp: ENSP00000448378.1:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1160C>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.347C>T
  hgvsp: ENSP00000449787.1:p.Thr116Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.155C>T
  hgvsp: ENSP00000447335.1:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.186C>T
  hgvsp: ENSP00000448910.1:p.Thr63Ile
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.321C>T
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13244
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28463
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr797Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-57909119-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909119
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909119
    reference: chr 12
allele count: 104
allele frequency: 9.100295759612187e-4
allele num: 114282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156A>C
  hgvsp: ENST00000552499.1:c.156A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689A>C
  hgvsp: ENST00000315473.5:c.1689A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.322A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1159A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154A>C
  hgvsp: ENST00000551172.1:c.154A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187A>C
  hgvsp: ENST00000547665.1:c.187A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348A>C
  hgvsp: ENST00000552914.1:c.348A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391A>C
  hgvsp: ENST00000262027.5:c.2391A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892A>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683A>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27459
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12852
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6882
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
hgvs: c.2391A>C
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

12-57909127-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909127
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909127
    reference: chr 12
allele count: 1
allele frequency: 8.974243919949743e-6
allele num: 111430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1151G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187+8G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.330G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689+8G>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4046
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2391+8G>C
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

12-57909148-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909148
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909148
    reference: chr 12
allele count: 5
allele frequency: 4.75520219119717e-5
allele num: 105148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1130A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.351A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892+29A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683+29A>G
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10219
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-57909151-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909151
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909151
    reference: chr 12
allele count: 1
allele frequency: 9.634468273695974e-6
allele num: 103794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.354G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1127G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156+32G>T
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154+32G>T
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20012
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

12-57909155-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909155
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909155
    reference: chr 12
allele count: 1
allele frequency: 9.826850887364635e-6
allele num: 101762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1123C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.358C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683+36C>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156+36C>G
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-57909163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909163
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909163
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 97046
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2391+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.156+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.348+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-1115A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.187+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.154+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*683+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1892+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1689+44A>G
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166986
  ensembl transcript: ENST00000551805
  gene symbol: MARS
  hgvsc: ENST00000551805.1:n.366A>G
  variant of: http://identifiers.org/hgnc/6898
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10547
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10140
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-57909653-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909653
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909653
    reference: chr 12
allele count: 4
allele frequency: 3.411746643694239e-5
allele num: 117242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*684-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.155-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1893-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2392-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.349-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1690-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-625G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.188-50G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.157-50G>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37000
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

12-57909656-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909656
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909656
    reference: chr 12
allele count: 3
allele frequency: 2.557850041778217e-5
allele num: 117286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1893-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1690-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*684-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2392-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.188-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-622G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.155-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.349-47G>A
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.157-47G>A
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

12-57909656-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909656
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909656
    reference: chr 12
allele count: 1
allele frequency: 8.526166805927391e-6
allele num: 117286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.188-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2392-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.349-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.155-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1893-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1690-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*684-47G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-622G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.157-47G>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37183
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-57909658-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909658
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909658
    reference: chr 12
allele count: 2
allele frequency: 1.705058909785333e-5
allele num: 117298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449071
  ensembl transcript: ENST00000548944
  gene symbol: MARS
  hgvsc: ENST00000548944.1:c.134-620G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448378
  ensembl transcript: ENST00000551172
  gene symbol: MARS
  hgvsc: ENST00000551172.1:c.155-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000314653
  ensembl transcript: ENST00000315473
  gene symbol: MARS
  hgvsc: ENST00000315473.5:c.1690-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000262027
  ensembl transcript: ENST00000262027
  gene symbol: MARS
  hgvsc: ENST00000262027.5:c.2392-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000449787
  ensembl transcript: ENST00000552914
  gene symbol: MARS
  hgvsc: ENST00000552914.1:c.349-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000439307
  ensembl transcript: ENST00000545888
  gene symbol: MARS
  hgvsc: ENST00000545888.2:c.*1893-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000446168
  ensembl transcript: ENST00000537638
  gene symbol: MARS
  hgvsc: ENST00000537638.2:c.*684-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000447335
  ensembl transcript: ENST00000552499
  gene symbol: MARS
  hgvsc: ENST00000552499.1:c.157-45G>C
  variant of: http://identifiers.org/hgnc/6898
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.188-45G>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

12-57909661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57909661
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 57909661
    reference: chr 12
allele count: 1
allele frequency: 8.519484060045324e-6
allele num: 117378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166986
  ensembl protein: ENSP00000448910
  ensembl transcript: ENST00000547665
  gene symbol: MARS
  hgvsc: ENST00000547665.1:c.188-42T>C
  variant of: http://identifiers.org/hgnc/6898
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33269
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7441
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7587
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 2.111217e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33290
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2871
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493106342165208e-5
allele num: 66728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.757e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

QD
type: SiteQuality
SIO_000300: 1.272e1

DP
type: SiteQuality
SIO_000300: 2.110621e6

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

GenotypeQuality
all individuals: 1927
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2674
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33282
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7508
bin: 9.75e1
variant carriers: 610

GenotypeQuality
all individuals: 2858
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7576
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.45366444579043e-3
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.554941257774706e-3
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 80
allele frequency: 1.209555488358029e-2
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 470
allele frequency: 7.043942209699658e-3
allele num: 66724
num of homozygotes: 1

African
type: Population
allele count: 9
allele frequency: 8.648856428983279e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 10
allele frequency: 1.101321585903084e-2
allele num: 908
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

DP
type: SiteQuality
SIO_000300: 2.112732e6

FS
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2664
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6942
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3456
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33626
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.676e0

DP
type: SiteQuality
SIO_000300: 2.090788e6

FS
type: SiteQuality
SIO_000300: 7.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.01e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 3.503e1

GenotypeQuality
all individuals: 7565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33601
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2855
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6942
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1936
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 2.315e0

VQSLOD
type: SiteQuality
SIO_000300: -1.707e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 2.090064e6

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2845
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

FS
type: SiteQuality
SIO_000300: 7.37e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

DP
type: SiteQuality
SIO_000300: 2.089068e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 2644
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33506
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3439
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7552
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.158e0

VQSLOD
type: SiteQuality
SIO_000300: -3.181e-1

DP
type: SiteQuality
SIO_000300: 2.08888e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.103e0

QD
type: SiteQuality
SIO_000300: 1.453e1

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.102e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 10
allele frequency: 9.611687812379854e-4
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 4.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 2.089009e6

GenotypeQuality
all individuals: 2624
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2828
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 33446
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6978
bin: 9.75e1
variant carriers: 255

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.048038707447727e-4
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.483820143012969e-4
allele num: 16502
num of homozygotes: 1

African
type: Population
allele count: 9
allele frequency: 8.652182272639877e-4
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 217
allele frequency: 3.253470868691715e-3
allele num: 66698
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.503e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
type: SiteQuality
SIO_000300: 2.089423e6

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33683
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.075e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 2.082326e6

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.443e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

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

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6761
bin: 9.75e1
variant carriers: 95

GenotypeQuality
all individuals: 2622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495352881213648e-5
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 86
allele frequency: 9.939898289412852e-3
allele num: 8652
num of homozygotes: 1

DP
type: SiteQuality
SIO_000300: 2.082007e6

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.185e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.96e-2

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6413
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.881e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.483e0

QD
type: SiteQuality
SIO_000300: 1.532e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.077445e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.162e0

GenotypeQuality
all individuals: 344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1739
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6956
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

QD
type: SiteQuality
SIO_000300: 1.578e1

DP
type: SiteQuality
SIO_000300: 2.077125e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 7.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.179e0

GenotypeQuality
all individuals: 1280
bin: 7.25e1
variant carriers: 41

GenotypeQuality
all individuals: 1327
bin: 9.75e1
variant carriers: 403

GenotypeQuality
all individuals: 1101
bin: 3.25e1
variant carriers: 60

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1334
bin: 4.75e1
variant carriers: 66

GenotypeQuality
all individuals: 598
bin: 8.25e1
variant carriers: 27

GenotypeQuality
all individuals: 722
bin: 7.5e0
variant carriers: 49

GenotypeQuality
all individuals: 1016
bin: 2.25e1
variant carriers: 70

GenotypeQuality
all individuals: 817
bin: 1.75e1
variant carriers: 61

GenotypeQuality
all individuals: 1192
bin: 7.75e1
variant carriers: 32

GenotypeQuality
all individuals: 1333
bin: 5.75e1
variant carriers: 51

GenotypeQuality
all individuals: 30626
bin: 6.25e1
variant carriers: 48

European (Finnish)
type: Population
allele count: 115
allele frequency: 3.048780487804878e-2
allele num: 3772
num of homozygotes: 0

African
type: Population
allele count: 155
allele frequency: 1.958059626073775e-2
allele num: 7916
num of homozygotes: 0

Latino
type: Population
allele count: 187
allele frequency: 2.297297297297297e-2
allele num: 8140
num of homozygotes: 0

East Asian
type: Population
allele count: 131
allele frequency: 1.89525462962963e-2
allele num: 6912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 508
allele frequency: 8.934224410833627e-3
allele num: 56860
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.492012779552716e-3
allele num: 15650
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 1.271186440677966e-2
allele num: 708
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.91e1

DP
type: SiteQuality
SIO_000300: 1.957294e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.027e0

VQSLOD
type: SiteQuality
SIO_000300: -9.353e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.83e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

FS
type: SiteQuality
SIO_000300: 1.42601e2

QD
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.388e0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7402
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 238
bin: 2.75e1
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: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.695059e6

VQSLOD
type: SiteQuality
SIO_000300: -2.196e1

QD
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 6.719799999999999e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 376
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 403
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7402
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 395
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1755
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1884
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 273
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.303898600348411e-4
allele num: 66588
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.677207867335133e-4
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.184291898577613e-4
allele num: 6468
num of homozygotes: 0

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

East Asian
type: Population
allele count: 13
allele frequency: 1.506024096385542e-3
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.735207357279195e-3
allele num: 11526
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.63901018922853e-4
allele num: 16488
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.196e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 6.719799999999999e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 1.695059e6

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 244
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7526
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.730403183941858e-4
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.083e0

QD
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.9526e1

DP
type: SiteQuality
SIO_000300: 1.69225e6

GenotypeQuality
all individuals: 7529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 998
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.155e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.386e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.691253e6

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
all individuals: 170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1762
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7559
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.276e0

QD
type: SiteQuality
SIO_000300: 1.013e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 1.276e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

DP
type: SiteQuality
SIO_000300: 1.69203e6

MQ
type: SiteQuality
SIO_000300: 5.551e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.301e1

DP
type: SiteQuality
SIO_000300: 1.692784e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

QD
type: SiteQuality
SIO_000300: 1.31e1

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.693317e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.696e0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 359
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7364
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 355
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 7.75e1
variant carriers: 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: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.781088082901554e-3
allele num: 6176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.699885e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e0

FS
type: SiteQuality
SIO_000300: 1.41057e2

VQSLOD
type: SiteQuality
SIO_000300: -9.07e1

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7575
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1835
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1802
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 1.683876e6

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

FS
type: SiteQuality
SIO_000300: 5.467e0

VQSLOD
type: SiteQuality
SIO_000300: 5.14e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1841
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 9.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49842555105713e-5
allele num: 66690
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.247e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 1.684736e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.63e-1

MQ
type: SiteQuality
SIO_000300: 5.585e1

QD
type: SiteQuality
SIO_000300: 1.695e1

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7556
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1834
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 42
allele frequency: 4.036908881199538e-3
allele num: 10404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

FS
type: SiteQuality
SIO_000300: 2.501e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

DP
type: SiteQuality
SIO_000300: 1.688885e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

FS
type: SiteQuality
SIO_000300: 2.501e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

DP
type: SiteQuality
SIO_000300: 1.688885e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.25e1

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46208
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1184
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7425
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516116316443798e-5
allele num: 65958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.101736972704715e-4
allele num: 6448
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.730039e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.337e-1

FS
type: SiteQuality
SIO_000300: 2.432e0

MQ
type: SiteQuality
SIO_000300: 5.839e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

QD
type: SiteQuality
SIO_000300: 1.352e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7311
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 481
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.149606299212598e-4
allele num: 6350
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: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.0823771608489e-5
allele num: 66062
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.97029702970297e-4
allele num: 10100
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e0

VQSLOD
type: SiteQuality
SIO_000300: -1.618e2

FS
type: SiteQuality
SIO_000300: 1.84812e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.031e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.74e0

MQ
type: SiteQuality
SIO_000300: 5.697e1

QD
type: SiteQuality
SIO_000300: 4.9e-1

DP
type: SiteQuality
SIO_000300: 1.69324e6

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7548
bin: 6.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.001980435695853e-5
allele num: 66652
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.269e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.274e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

FS
type: SiteQuality
SIO_000300: 1.122e0

DP
type: SiteQuality
SIO_000300: 1.667752e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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

GenotypeQuality
all individuals: 799
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00048007681229e-5
allele num: 66656
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.663e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.58e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.201e-1

DP
type: SiteQuality
SIO_000300: 1.667192e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.078e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.35e-1

QD
type: SiteQuality
SIO_000300: 1.645e1

GenotypeDepth
all individuals: 583
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7547
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47164
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 957
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 797
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.416e1

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 1.666612e6

FS
type: SiteQuality
SIO_000300: 6.471e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.242e0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 47198
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1779
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7552
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.666585e6

MQ
type: SiteQuality
SIO_000300: 5.481e1

FS
type: SiteQuality
SIO_000300: 5.418e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.236e0

VQSLOD
type: SiteQuality
SIO_000300: -1.027e0

QD
type: SiteQuality
SIO_000300: 1.592e1

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7562
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 957
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

FS
type: SiteQuality
SIO_000300: 4.187e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.539e0

QD
type: SiteQuality
SIO_000300: 1.194e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.662875e6

GenotypeDepth
all individuals: 37
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7564
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 47279
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.494454103963068e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.663168e6

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.937e1

QD
type: SiteQuality
SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.278e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

GenotypeDepth
all individuals: 21
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47279
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7564
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 962
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 7.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.278e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.663168e6

GenotypeDepth
all individuals: 31
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 951
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47304
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.662463e6

FS
type: SiteQuality
SIO_000300: 3.534e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.66e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.004e1

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 792
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 951
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.588e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.131e-1

FS
type: SiteQuality
SIO_000300: 8.853999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.66243e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.47e-1

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

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 952
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47298
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1677
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.662514e6

FS
type: SiteQuality
SIO_000300: 7.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.269e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 1.588e1

GenotypeDepth
all individuals: 107
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47299
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7559
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.49e-1

DP
type: SiteQuality
SIO_000300: 1.662379e6

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 1.893e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.372e0

GenotypeDepth
all individuals: 54
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47303
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1677
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7552
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.954e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.164e1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.662376e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeDepth
all individuals: 35
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1768
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 949
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47290
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.661999e6

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

VQSLOD
type: SiteQuality
SIO_000300: -3.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.35e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 25
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7549
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 47290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49707690001499e-5
allele num: 66710
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.842e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

QD
type: SiteQuality
SIO_000300: 1.27e1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

DP
type: SiteQuality
SIO_000300: 1.662081e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.917e1

GenotypeDepth
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7546
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1672
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 47284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.441e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.589e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 1.661915e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.789e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 8.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 786
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.661917e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.415e0

FS
type: SiteQuality
SIO_000300: 1.714e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.006e1

GenotypeDepth
all individuals: 36
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47272
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 949
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 784
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-1

FS
type: SiteQuality
SIO_000300: 6.288e0

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 1.661744e6

GenotypeDepth
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47286
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 947
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.492e1

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

FS
type: SiteQuality
SIO_000300: 2.669e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

DP
type: SiteQuality
SIO_000300: 1.661741e6

GenotypeQuality
all individuals: 1668
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7539
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

QD
type: SiteQuality
SIO_000300: 1.231e1

FS
type: SiteQuality
SIO_000300: 1.749e0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.661483e6

GenotypeQuality
all individuals: 1764
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7536
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 945
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.661066e6

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

FS
type: SiteQuality
SIO_000300: 1.091e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.574e0

VQSLOD
type: SiteQuality
SIO_000300: -1.432e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQ
type: SiteQuality
SIO_000300: 5.664e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeQuality
all individuals: 47274
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.731e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.661083e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.578e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.314e0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
all individuals: 1659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47252
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7537
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.660517e6

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 9.87e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.563e0

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

QD
type: SiteQuality
SIO_000300: 1.396e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.451e0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1640
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47004
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1718
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.095e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
SIO_000300: 6.79e0

MQRankSum
type: SiteQuality
SIO_000300: 9.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

DP
type: SiteQuality
SIO_000300: 1.656917e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.863e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47071
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
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: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.557e0

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.654621e6

MQ
type: SiteQuality
SIO_000300: 5.905e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1687
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47080
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.214771622934888e-4
allele num: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.104e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 1.654366e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 2.597e0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 738
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 46921
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e0

DP
type: SiteQuality
SIO_000300: 1.647311e6

VQSLOD
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 912
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7081
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46790
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.044e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.35e0

QD
type: SiteQuality
SIO_000300: 1.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.032e0

FS
type: SiteQuality
SIO_000300: 9.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.106e0

VQSLOD
type: SiteQuality
SIO_000300: -1.597e0

DP
type: SiteQuality
SIO_000300: 1.637878e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 6976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1080
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46387
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
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: 16326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.071940488070398e-5
allele num: 66138
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.194e0

QD
type: SiteQuality
SIO_000300: 1.299e1

DP
type: SiteQuality
SIO_000300: 1.628291e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.372479240806643e-4
allele num: 8430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15848
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64398
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.89e-1

DP
type: SiteQuality
SIO_000300: 1.538994e6

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1073
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5653
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42293
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10928
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023541453428864e-4
allele num: 9770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63956
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.777e1

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: -1.643e0

DP
type: SiteQuality
SIO_000300: 1.518827e6

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 1.1856e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.567e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.679e0

GenotypeDepth
all individuals: 7138
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1173
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5466
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6648
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.133553173948887e-3
allele num: 9704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.479e0

FS
type: SiteQuality
SIO_000300: 7.419e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.14e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.491064e6

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

GenotypeDepth
all individuals: 34
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 865
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1353
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 9.75e1
variant carriers: 100

GenotypeQuality
all individuals: 38835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7687
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.352941176470588e-3
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 82
allele frequency: 1.301917947415216e-3
allele num: 62984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.117854915817917e-4
allele num: 9622
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.862495171881035e-4
allele num: 15534
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.019651464590285e-3
allele num: 10788
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 1.465084e6

FS
type: SiteQuality
SIO_000300: 5.45e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.292e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11258
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 380
bin: 4.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.616382162233691e-5
allele num: 15114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.97e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 4.712e0

DP
type: SiteQuality
SIO_000300: 1.370387e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.15e-1

QD
type: SiteQuality
SIO_000300: 1.632e1

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5922
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7745
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19834
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3957
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8814
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.109339873288372e-4
allele num: 9786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
SIO_000300: 1.474e1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 1.043388e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.546e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

GenotypeQuality
all individuals: 1073
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6301
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4925
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.744957074055978e-5
allele num: 57308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8690
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.666e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

FS
type: SiteQuality
SIO_000300: 3.786e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.51e-1

QD
type: SiteQuality
SIO_000300: 1.343e1

DP
type: SiteQuality
SIO_000300: 9.98138e5

GenotypeQuality
all individuals: 441
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9595
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19817
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5859
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.777840989901863e-5
allele num: 56248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 1.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.299e0

FS
type: SiteQuality
SIO_000300: 4.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 9.57369e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

GenotypeQuality
all individuals: 810
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7050
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6866
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13208
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 8.97938e5

VQSLOD
type: SiteQuality
SIO_000300: -2.493e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

QD
type: SiteQuality
SIO_000300: 1.466e1

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.707e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1023
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65678
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.892263195950832e-4
allele num: 13830
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 9.625999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.265e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.012e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.710146e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

GenotypeQuality
all individuals: 2138
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9205
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.567044208987943e-5
allele num: 65688
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13862
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.533e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

DP
type: SiteQuality
SIO_000300: 1.710691e6

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.75e1
variant carriers: 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: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522348069662648e-5
allele num: 65688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13862
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.710691e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 1.533e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.075e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1112
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.044788843893676e-5
allele num: 65686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.586e-1

FS
type: SiteQuality
SIO_000300: 7.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.299e1

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

DP
type: SiteQuality
SIO_000300: 1.710975e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

MQ
type: SiteQuality
SIO_000300: 6.0e1