6-24418388-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418388
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418388
    reference: chr 6
allele count: 9
allele frequency: 7.414730598121601e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*446G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.40G>T
  hgvsp: ENSP00000438118.1:p.Asp14Tyr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.913G>T
  hgvsp: ENSP00000367637.3:p.Asp305Tyr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.913G>T
  hgvsp: ENSP00000367604.1:p.Asp305Tyr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.763G>T
  hgvsp: ENSP00000441839.1:p.Asp255Tyr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.893G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.369G>T
  hgvsp: ENSP00000387441.1:p.Asp124Tyr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.922G>T
  hgvsp: ENSP00000399585.2:p.Asp308Tyr
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp305Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

6-24418388-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418388
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418388
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.40G>A
  hgvsp: ENSP00000438118.1:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.763G>A
  hgvsp: ENSP00000441839.1:p.Asp255Asn
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.369G>A
  hgvsp: ENSP00000387441.1:p.Asp124Asn
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*446G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.893G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.922G>A
  hgvsp: ENSP00000399585.2:p.Asp308Asn
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.913G>A
  hgvsp: ENSP00000367637.3:p.Asp305Asn
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.913G>A
  hgvsp: ENSP00000367604.1:p.Asp305Asn
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp305Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/6-24418389-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418389
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418389
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*447A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.41A>C
  hgvsp: ENSP00000438118.1:p.Asp14Ala
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.764A>C
  hgvsp: ENSP00000441839.1:p.Asp255Ala
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.370A>C
  hgvsp: ENSP00000387441.1:p.Asp124Ala
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.894A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.914A>C
  hgvsp: ENSP00000367604.1:p.Asp305Ala
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.923A>C
  hgvsp: ENSP00000399585.2:p.Asp308Ala
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.914A>C
  hgvsp: ENSP00000367637.3:p.Asp305Ala
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp305Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-24418398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418398
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418398
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*456A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.903A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.923A>G
  hgvsp: ENSP00000367604.1:p.Asn308Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.379A>G
  hgvsp: ENSP00000387441.1:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.923A>G
  hgvsp: ENSP00000367637.3:p.Asn308Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.932A>G
  hgvsp: ENSP00000399585.2:p.Asn311Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.773A>G
  hgvsp: ENSP00000441839.1:p.Asn258Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.50A>G
  hgvsp: ENSP00000438118.1:p.Asn17Ser
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn308Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

6-24418399-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418399
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418399
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*457T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.380T>C
  hgvsp: ENST00000446191.1:c.380T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.51T>C
  hgvsp: ENST00000543597.1:c.51T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.904T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.774T>C
  hgvsp: ENST00000535061.1:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.924T>C
  hgvsp: ENST00000378386.3:c.924T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.933T>C
  hgvsp: ENST00000443868.2:c.933T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.924T>C
  hgvsp: ENST00000378353.1:c.924T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42762
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn308Asn
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

6-24418401-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418401
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418401
    reference: chr 6
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.776C>G
  hgvsp: ENSP00000441839.1:p.Ala259Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.906C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.382C>G
  hgvsp: ENSP00000387441.1:p.Ala128Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.926C>G
  hgvsp: ENSP00000367637.3:p.Ala309Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.935C>G
  hgvsp: ENSP00000399585.2:p.Ala312Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.926C>G
  hgvsp: ENSP00000367604.1:p.Ala309Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*459C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.53C>G
  hgvsp: ENSP00000438118.1:p.Ala18Gly
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11179
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala309Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-24418407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418407
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418407
    reference: chr 6
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.388G>A
  hgvsp: ENSP00000387441.1:p.Arg130His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.941G>A
  hgvsp: ENSP00000399585.2:p.Arg314His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.782G>A
  hgvsp: ENSP00000441839.1:p.Arg261His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*465G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.932G>A
  hgvsp: ENSP00000367637.3:p.Arg311His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.932G>A
  hgvsp: ENSP00000367604.1:p.Arg311His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.912G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.59G>A
  hgvsp: ENSP00000438118.1:p.Arg20His
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg311His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

6-24418441-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418441
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418441
    reference: chr 6
allele count: 2
allele frequency: 1.650955077512341e-5
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.966T>A
  hgvsp: ENSP00000367604.1:p.Ser322Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.966T>A
  hgvsp: ENSP00000367637.3:p.Ser322Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.93T>A
  hgvsp: ENSP00000438118.1:p.Ser31Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.816T>A
  hgvsp: ENSP00000441839.1:p.Ser272Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.946T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.975T>A
  hgvsp: ENSP00000399585.2:p.Ser325Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.422T>A
  hgvsp: ENSP00000387441.1:p.Ser141Arg
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*499T>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser322Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-24418442-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418442
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418442
    reference: chr 6
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.976A>G
  hgvsp: ENSP00000399585.2:p.Ile326Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.423A>G
  hgvsp: ENSP00000387441.1:p.Ile142Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.817A>G
  hgvsp: ENSP00000441839.1:p.Ile273Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.967A>G
  hgvsp: ENSP00000367604.1:p.Ile323Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*500A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.94A>G
  hgvsp: ENSP00000438118.1:p.Ile32Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.967A>G
  hgvsp: ENSP00000367637.3:p.Ile323Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.947A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile323Val
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

6-24418455-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418455
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418455
    reference: chr 6
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.107A>G
  hgvsp: ENSP00000438118.1:p.Asn36Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.980A>G
  hgvsp: ENSP00000367604.1:p.Asn327Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.980A>G
  hgvsp: ENSP00000367637.3:p.Asn327Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.830A>G
  hgvsp: ENSP00000441839.1:p.Asn277Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.960A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.436A>G
  hgvsp: ENSP00000387441.1:p.Asn146Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*513A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.989A>G
  hgvsp: ENSP00000399585.2:p.Asn330Ser
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn327Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-24418462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418462
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418462
    reference: chr 6
allele count: 1
allele frequency: 8.327920185212944e-6
allele num: 120078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.443C>T
  hgvsp: ENST00000446191.1:c.443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*520C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.996C>T
  hgvsp: ENST00000443868.2:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.967C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.987C>T
  hgvsp: ENST00000378386.3:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.987C>T
  hgvsp: ENST00000378353.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.837C>T
  hgvsp: ENST00000535061.1:c.837C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.114C>T
  hgvsp: ENST00000543597.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
hgvs: c.987C>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-24418463-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418463
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418463
    reference: chr 6
allele count: 1
allele frequency: 8.343763037129745e-6
allele num: 119850
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.988A>G
  hgvsp: ENSP00000367637.3:p.Ser330Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*521A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.444A>G
  hgvsp: ENSP00000387441.1:p.Ser149Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.838A>G
  hgvsp: ENSP00000441839.1:p.Ser280Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.968A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.997A>G
  hgvsp: ENSP00000399585.2:p.Ser333Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.115A>G
  hgvsp: ENSP00000438118.1:p.Ser39Gly
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.988A>G
  hgvsp: ENSP00000367604.1:p.Ser330Gly
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1769
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10590
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39413
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser330Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

6-24418472-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418472
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418472
    reference: chr 6
allele count: 1
allele frequency: 8.487379267029927e-6
allele num: 117822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+8A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+8A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 2.75e1
  variant carriers: 0
hgvs: c.989+8A>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-24418473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418473
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418473
    reference: chr 6
allele count: 1
allele frequency: 8.489252606200551e-6
allele num: 117796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+9G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+9G>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-24418479-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418479
    reference: chr 6
allele count: 1
allele frequency: 8.683269077142163e-6
allele num: 115164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+15T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+15T>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

6-24418480-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418480
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418480
    reference: chr 6
allele count: 1
allele frequency: 8.733014287211374e-6
allele num: 114508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+16A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+16A>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12169
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2630
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

6-24418481-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418481
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418481
    reference: chr 6
allele count: 2
allele frequency: 1.779359430604982e-5
allele num: 112400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+17T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+17T>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10264
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19019
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-24418485-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418485
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418484
    reference: chr 6
allele count: 1
allele frequency: 9.217609320846545e-6
allele num: 108488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+22delC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+22delC
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: AC
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

6-24418486-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418486
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418487
    reference: chr 6
allele count: 2
allele frequency: 1.871993111065351e-5
allele num: 106838
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+23dupT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+23dupT
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4052
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-24418486-CTAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418486
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418482
    reference: chr 6
allele count: 1
allele frequency: 9.359965555326756e-6
allele num: 106838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+24_116+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+24_839+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+24_998+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+24_445+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+24_989+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+24_989+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+24_*522+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+24_969+27delAAGT
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8195
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4052
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: CTAAG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

6-24418487-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418489
    reference: chr 6
allele count: 3
allele frequency: 3.041794253036724e-5
allele num: 98626
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+24_445+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+24_998+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+24_989+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+24_*522+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+24_969+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+24_116+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+24_839+25dupAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+24_989+25dupAA
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-24418489-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418489
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418489
    reference: chr 6
allele count: 1
allele frequency: 1.011981865284974e-5
allele num: 98816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+25A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+25A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12309
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7046
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20654
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

6-24418494-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418494
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418494
    reference: chr 6
allele count: 28
allele frequency: 3.156565656565657e-4
allele num: 88704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+30T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+30T>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11301
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15158
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9088
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 17060
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-24418497-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418497
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418497
    reference: chr 6
allele count: 2
allele frequency: 2.594572155051632e-5
allele num: 77084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+33T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+33T>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2498
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9141
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-24418500-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418500
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418497
    reference: chr 6
allele count: 1
allele frequency: 1.35000135000135e-5
allele num: 74074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+38_839+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+38_989+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+38_969+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+38_445+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+38_998+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+38_989+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+38_116+40delAAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+38_*522+40delAAA
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: TAAA
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-24418502-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418502
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418502
    reference: chr 6
allele count: 26868
allele frequency: 3.549461001902346e-1
allele num: 75696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+38A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+38A>C
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 391
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 769
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 1.25e1
  variant carriers: 5301
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 1602
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 11177
  bin: 7.5e0
  variant carriers: 3899
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.5e0
  variant carriers: 519
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 10474
  bin: 1.75e1
  variant carriers: 5449
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 2.25e1
  variant carriers: 4564
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 2.75e1
  variant carriers: 3045
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 6098
  bin: 7.5e0
  variant carriers: 263
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 718
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 1.25e1
  variant carriers: 375
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 498
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 2.5e0
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 4.75e1
  variant carriers: 673
genotype quality: GenotypeQuality
  all individuals: 17860
  bin: 9.75e1
  variant carriers: 17108
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.75e1
  variant carriers: 549
num of homozygotes: 4949
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

6-24418503-AATAATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418503
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418497
    reference: chr 6
allele count: 2
allele frequency: 2.889087914945252e-5
allele num: 69226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+44_839+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+44_989+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+44_116+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+44_998+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+44_*522+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+44_445+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+44_969+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+44_989+49delTTATAA
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16065
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3352
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12879
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: AATAATT
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

6-24418504-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418504
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418504
    reference: chr 6
allele count: 1
allele frequency: 1.439553162698298e-5
allele num: 69466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+40A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+40A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4214
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3642
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10090
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-24418505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418505
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418505
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 68762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+41T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+41T>C
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8298
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-24418506-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418506
    reference: chr 6
allele count: 1
allele frequency: 1.457598460776025e-5
allele num: 68606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+42A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+42A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9934
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3952
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11260
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3310
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-24418506-AATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418506
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418503
    reference: chr 6
allele count: 2255
allele frequency: 3.286884529049938e-2
allele num: 68606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+45_445+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+45_839+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+45_*522+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+45_116+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+45_989+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+45_989+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+45_998+47delTAT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+45_969+47delTAT
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 9934
  bin: 1.75e1
  variant carriers: 615
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 3.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 2.25e1
  variant carriers: 404
genotype depth: GenotypeDepth
  all individuals: 8608
  bin: 2.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 13270
  bin: 7.5e0
  variant carriers: 477
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15111
  bin: 1.25e1
  variant carriers: 705
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 9319
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2262
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 11260
  bin: 2.25e1
  variant carriers: 11
num of homozygotes: 36
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AATT
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

6-24418510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418510
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418510
    reference: chr 6
allele count: 1
allele frequency: 1.571981010469394e-5
allele num: 63614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+46A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+46A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9384
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3258
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9991
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3604
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5649
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

6-24418510-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418510
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418510
    reference: chr 6
allele count: 6
allele frequency: 9.431886062816361e-5
allele num: 63614
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+46A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+46A>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14255
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9384
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3258
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5649
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-24418511-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
allele count: 1
allele frequency: 1.519572088499878e-5
allele num: 65808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+47T>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+47T>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-24418511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
allele count: 1
allele frequency: 1.519572088499878e-5
allele num: 65808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+47T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+47T>C
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

6-24418511-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418510
    reference: chr 6
allele count: 498
allele frequency: 7.567469000729394e-3
allele num: 65808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+49delA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+49delA
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14389
  bin: 1.25e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 1.75e1
  variant carriers: 136
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14257
  bin: 7.5e0
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 10194
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 9.75e1
  variant carriers: 478
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11463
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 9.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 19
num of homozygotes: 10
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: TA
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

6-24418511-TAAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418511
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418507
    reference: chr 6
allele count: 3
allele frequency: 4.558716265499635e-5
allele num: 65808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.839+51_839+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.116+51_116+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.989+51_989+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.445+51_445+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*522+51_*522+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.998+51_998+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.969+51_969+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.989+51_989+54delAAAG
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14257
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14389
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5813
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: TAAGA
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

6-24418639-GTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418639
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418637
    reference: chr 6
allele count: 2
allele frequency: 1.653275138048474e-5
allele num: 120972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-45_990-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-45_117-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-45_999-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-45_446-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-45_990-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-45_840-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-45_*523-44delTA
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-45_970-44delTA
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49273
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: GTA
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-24418641-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418641
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418641
    reference: chr 6
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-48A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-48A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
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: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-24418643-ATAGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418643
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418639
    reference: chr 6
allele count: 2
allele frequency: 1.652537471287161e-5
allele num: 121026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-41_*523-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-41_990-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-41_446-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-41_999-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-41_990-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-41_970-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-41_840-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-41_117-38delTAGT
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: ATAGT
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

6-24418650-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418650
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418650
    reference: chr 6
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-39G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-39G>C
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

6-24418667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418667
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418667
    reference: chr 6
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-22G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-22G>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

6-24418677-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418677
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418674
    reference: chr 6
allele count: 67
allele frequency: 5.524406332453826e-4
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-8_117-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-8_446-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-8_999-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-8_990-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-8_*523-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-8_970-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-8_990-6delCTC
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-8_840-6delCTC
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: TCTC
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

6-24418680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418680
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418680
    reference: chr 6
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-9C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-9C>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

6-24418685-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418685
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418685
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-4C>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-4C>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: c.990-4C>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-24418685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418685
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418685
    reference: chr 6
allele count: 15
allele frequency: 1.236256943643167e-4
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.446-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.990-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.840-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.990-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*523-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.117-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.970-4C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.999-4C>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
hgvs: c.990-4C>T
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-24418692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418692
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418692
    reference: chr 6
allele count: 6
allele frequency: 4.943561011782154e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.993C>T
  hgvsp: ENST00000378386.3:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*526C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.973C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.120C>T
  hgvsp: ENST00000543597.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1002C>T
  hgvsp: ENST00000443868.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.843C>T
  hgvsp: ENST00000535061.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.993C>T
  hgvsp: ENST00000378353.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.449C>T
  hgvsp: ENST00000446191.1:c.449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5372
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His331His
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-24418693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418693
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418693
    reference: chr 6
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1003C>T
  hgvsp: ENSP00000399585.2:p.Arg335Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.844C>T
  hgvsp: ENSP00000441839.1:p.Arg282Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.994C>T
  hgvsp: ENSP00000367637.3:p.Arg332Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.121C>T
  hgvsp: ENSP00000438118.1:p.Arg41Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.994C>T
  hgvsp: ENSP00000367604.1:p.Arg332Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.450C>T
  hgvsp: ENSP00000387441.1:p.Arg151Ter
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.974C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*527C>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg332Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

6-24418698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418698
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418698
    reference: chr 6
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.979C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.999C>T
  hgvsp: ENST00000378386.3:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*532C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.126C>T
  hgvsp: ENST00000543597.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.849C>T
  hgvsp: ENST00000535061.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.999C>T
  hgvsp: ENST00000378353.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.455C>T
  hgvsp: ENST00000446191.1:c.455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1008C>T
  hgvsp: ENST00000443868.2:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn333Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-24418699-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418699
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418699
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.980G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1000G>A
  hgvsp: ENSP00000367604.1:p.Val334Met
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.127G>A
  hgvsp: ENSP00000438118.1:p.Val43Met
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1000G>A
  hgvsp: ENSP00000367637.3:p.Val334Met
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.850G>A
  hgvsp: ENSP00000441839.1:p.Val284Met
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.456G>A
  hgvsp: ENSP00000387441.1:p.Val153Met
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*533G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1009G>A
  hgvsp: ENSP00000399585.2:p.Val337Met
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val334Met
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-24418705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418705
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418705
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.462A>G
  hgvsp: ENSP00000387441.1:p.Met155Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1015A>G
  hgvsp: ENSP00000399585.2:p.Met339Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1006A>G
  hgvsp: ENSP00000367637.3:p.Met336Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.133A>G
  hgvsp: ENSP00000438118.1:p.Met45Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.856A>G
  hgvsp: ENSP00000441839.1:p.Met286Val
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.986A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*539A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1006A>G
  hgvsp: ENSP00000367604.1:p.Met336Val
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met336Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

6-24418705-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418705
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418705
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.856A>T
  hgvsp: ENSP00000441839.1:p.Met286Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.462A>T
  hgvsp: ENSP00000387441.1:p.Met155Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1006A>T
  hgvsp: ENSP00000367604.1:p.Met336Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.133A>T
  hgvsp: ENSP00000438118.1:p.Met45Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*539A>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1006A>T
  hgvsp: ENSP00000367637.3:p.Met336Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1015A>T
  hgvsp: ENSP00000399585.2:p.Met339Leu
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.986A>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met336Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-24418708-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418708
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418708
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.136A>C
  hgvsp: ENST00000543597.1:c.136A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.989A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*542A>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.465A>C
  hgvsp: ENST00000446191.1:c.465A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1009A>C
  hgvsp: ENST00000378353.1:c.1009A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1009A>C
  hgvsp: ENST00000378386.3:c.1009A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.859A>C
  hgvsp: ENST00000535061.1:c.859A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1018A>C
  hgvsp: ENST00000443868.2:c.1018A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg337Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-24418709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418709
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418709
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1010G>A
  hgvsp: ENSP00000367604.1:p.Arg337Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.990G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.466G>A
  hgvsp: ENSP00000387441.1:p.Arg156Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.860G>A
  hgvsp: ENSP00000441839.1:p.Arg287Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1010G>A
  hgvsp: ENSP00000367637.3:p.Arg337Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1019G>A
  hgvsp: ENSP00000399585.2:p.Arg340Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.137G>A
  hgvsp: ENSP00000438118.1:p.Arg46Lys
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*543G>A
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg337Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-24418710-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418710
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418710
    reference: chr 6
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.467G>C
  hgvsp: ENSP00000387441.1:p.Arg156Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.861G>C
  hgvsp: ENSP00000441839.1:p.Arg287Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1011G>C
  hgvsp: ENSP00000367637.3:p.Arg337Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.991G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.138G>C
  hgvsp: ENSP00000438118.1:p.Arg46Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1011G>C
  hgvsp: ENSP00000367604.1:p.Arg337Ser
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*544G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1020G>C
  hgvsp: ENSP00000399585.2:p.Arg340Ser
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49302
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg337Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

6-24418722-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418722
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418722
    reference: chr 6
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1003G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1023G>C
  hgvsp: ENSP00000367604.1:p.Gln341His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.873G>C
  hgvsp: ENSP00000441839.1:p.Gln291His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.479G>C
  hgvsp: ENSP00000387441.1:p.Gln160His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*556G>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.150G>C
  hgvsp: ENSP00000438118.1:p.Gln50His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1023G>C
  hgvsp: ENSP00000367637.3:p.Gln341His
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1032G>C
  hgvsp: ENSP00000399585.2:p.Gln344His
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln341His
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

6-24418727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418727
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418727
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1037C>T
  hgvsp: ENSP00000399585.2:p.Thr346Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1028C>T
  hgvsp: ENSP00000367637.3:p.Thr343Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1008C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.484C>T
  hgvsp: ENSP00000387441.1:p.Thr162Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*561C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1028C>T
  hgvsp: ENSP00000367604.1:p.Thr343Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.155C>T
  hgvsp: ENSP00000438118.1:p.Thr52Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.878C>T
  hgvsp: ENSP00000441839.1:p.Thr293Ile
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr343Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-24418728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418728
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418728
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.485C>T
  hgvsp: ENST00000446191.1:c.485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.879C>T
  hgvsp: ENST00000535061.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*562C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1038C>T
  hgvsp: ENST00000443868.2:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1029C>T
  hgvsp: ENST00000378386.3:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.156C>T
  hgvsp: ENST00000543597.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1029C>T
  hgvsp: ENST00000378353.1:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1009C>T
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr343Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ

6-24418730-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418730
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418730
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1040T>C
  hgvsp: ENSP00000399585.2:p.Met347Thr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.158T>C
  hgvsp: ENSP00000438118.1:p.Met53Thr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1011T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1031T>C
  hgvsp: ENSP00000367604.1:p.Met344Thr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.881T>C
  hgvsp: ENSP00000441839.1:p.Met294Thr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1031T>C
  hgvsp: ENSP00000367637.3:p.Met344Thr
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*564T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.487T>C
  hgvsp: ENSP00000387441.1:p.Met163Thr
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49299
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met344Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-24418736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418736
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418736
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.887C>T
  hgvsp: ENSP00000441839.1:p.Thr296Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1037C>T
  hgvsp: ENSP00000367637.3:p.Thr346Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1046C>T
  hgvsp: ENSP00000399585.2:p.Thr349Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.164C>T
  hgvsp: ENSP00000438118.1:p.Thr55Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1017C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.493C>T
  hgvsp: ENSP00000387441.1:p.Thr165Ile
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*570C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1037C>T
  hgvsp: ENSP00000367604.1:p.Thr346Ile
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5432
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr346Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-24418737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418737
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418737
    reference: chr 6
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*571C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1038C>T
  hgvsp: ENST00000378353.1:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.165C>T
  hgvsp: ENST00000543597.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1018C>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1038C>T
  hgvsp: ENST00000378386.3:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.494C>T
  hgvsp: ENST00000446191.1:c.494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.888C>T
  hgvsp: ENST00000535061.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1047C>T
  hgvsp: ENST00000443868.2:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49299
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr346Thr
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-24418746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418746
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418746
    reference: chr 6
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1027T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*580T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1056T>C
  hgvsp: ENST00000443868.2:c.1056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.503T>C
  hgvsp: ENST00000446191.1:c.503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1047T>C
  hgvsp: ENST00000378386.3:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.174T>C
  hgvsp: ENST00000543597.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1047T>C
  hgvsp: ENST00000378353.1:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.897T>C
  hgvsp: ENST00000535061.1:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu349Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-24418749-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418749
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418749
    reference: chr 6
allele count: 154
allele frequency: 1.26847108050673e-3
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*583G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1050G>A
  hgvsp: ENST00000378386.3:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.506G>A
  hgvsp: ENST00000446191.1:c.506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1050G>A
  hgvsp: ENST00000378353.1:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.177G>A
  hgvsp: ENST00000543597.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1059G>A
  hgvsp: ENST00000443868.2:c.1059G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1030G>A
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.900G>A
  hgvsp: ENST00000535061.1:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 9.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3760
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser350Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

6-24418783-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418783
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418783
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.540A>G
  hgvsp: ENSP00000387441.1:p.Asn181Asp
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1084A>G
  hgvsp: ENSP00000367637.3:p.Asn362Asp
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*617A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.934A>G
  hgvsp: ENSP00000441839.1:p.Asn312Asp
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1084A>G
  hgvsp: ENSP00000367604.1:p.Asn362Asp
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1064A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.211A>G
  hgvsp: ENSP00000438118.1:p.Asn71Asp
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1093A>G
  hgvsp: ENSP00000399585.2:p.Asn365Asp
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn362Asp
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: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-24418785-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418785
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418785
    reference: chr 6
allele count: 8
allele frequency: 6.589894396942289e-5
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.936T>C
  hgvsp: ENST00000535061.1:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*619T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1095T>C
  hgvsp: ENST00000443868.2:c.1095T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1086T>C
  hgvsp: ENST00000378353.1:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.542T>C
  hgvsp: ENST00000446191.1:c.542T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.213T>C
  hgvsp: ENST00000543597.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1066T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1086T>C
  hgvsp: ENST00000378386.3:c.1086T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn362Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

6-24418786-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418786
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418786
    reference: chr 6
allele count: 17650
allele frequency: 1.453919404263732e-1
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.214T>C
  hgvsp: ENST00000543597.1:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.937T>C
  hgvsp: ENST00000535061.1:c.937T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1087T>C
  hgvsp: ENST00000378353.1:c.1087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*620T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1067T>C
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1087T>C
  hgvsp: ENST00000378386.3:c.1087T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000387441
  ensembl transcript: ENST00000446191
  gene symbol: MRS2
  hgvsc: ENST00000446191.1:c.543T>C
  hgvsp: ENST00000446191.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1096T>C
  hgvsp: ENST00000443868.2:c.1096T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 7.25e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 5.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 7.75e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 8.75e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 4.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 6.25e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4676
  bin: 5.75e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 9.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 6.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 17660
  bin: 9.75e1
  variant carriers: 14311
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50992
  bin: 9.75e1
  variant carriers: 16142
hgvs: p.Leu363Leu
num of homozygotes: 1503
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

6-24418803-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418803
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418803
    reference: chr 6
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*637A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1084A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.954A>G
  hgvsp: ENST00000535061.1:c.954A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1113A>G
  hgvsp: ENST00000443868.2:c.1113A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1104A>G
  hgvsp: ENST00000378353.1:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.231A>G
  hgvsp: ENST00000543597.1:c.231A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1104A>G
  hgvsp: ENST00000378386.3:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu368Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

6-24418813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418813
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418813
    reference: chr 6
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1116+7A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.234+7A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1094A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1107+7A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*640+7A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1107+7A>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.957+7A>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1107+7A>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

6-24418814-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418814
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418814
    reference: chr 6
allele count: 2
allele frequency: 1.651336757104876e-5
allele num: 121114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.957+8T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1095T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*640+8T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.234+8T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1116+8T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1107+8T>G
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1107+8T>G
  variant of: http://identifiers.org/hgnc/13785
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11408
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42911
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2030
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1107+8T>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-24418815-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418815
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418815
    reference: chr 6
allele count: 2
allele frequency: 1.651391297167864e-5
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1107+9G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1116+9G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.957+9G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1107+9G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*640+9G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1096G>T
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.234+9G>T
  variant of: http://identifiers.org/hgnc/13785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42911
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

6-24418815-GTAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24418815
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 24418812
    reference: chr 6
allele count: 4
allele frequency: 3.302782594335728e-5
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000399585
  ensembl transcript: ENST00000443868
  gene symbol: MRS2
  hgvsc: ENST00000443868.2:c.1116+17_1116+19delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000274747
  ensembl transcript: ENST00000274747
  gene symbol: MRS2
  hgvsc: ENST00000274747.7:c.*640+17_*640+19delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367637
  ensembl transcript: ENST00000378386
  gene symbol: MRS2
  hgvsc: ENST00000378386.3:c.1107+17_1107+19delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000367604
  ensembl transcript: ENST00000378353
  gene symbol: MRS2
  hgvsc: ENST00000378353.1:c.1107+17_1107+19delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000441839
  ensembl transcript: ENST00000535061
  gene symbol: MRS2
  hgvsc: ENST00000535061.1:c.957+17_957+19delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124532
  ensembl transcript: ENST00000483634
  gene symbol: MRS2
  hgvsc: ENST00000483634.1:n.1104_1106delATT
  variant of: http://identifiers.org/hgnc/13785
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124532
  ensembl protein: ENSP00000438118
  ensembl transcript: ENST00000543597
  gene symbol: MRS2
  hgvsc: ENST00000543597.1:c.234+17_234+19delATT
  variant of: http://identifiers.org/hgnc/13785
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: GTAT

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11180
bin: 6.75e1
variant carriers: 0

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

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

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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049286485190071e-4
allele num: 66712
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.182e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

DP
type: SiteQuality
SIO_000300: 1.995672e6

QD
type: SiteQuality
SIO_000300: 1.222e1

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42759
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.995672e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.182e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 9.210000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 1.994901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 2.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11179
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
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: 8654
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

DP
type: SiteQuality
SIO_000300: 1.994822e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.409e1

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

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.388e0

DP
type: SiteQuality
SIO_000300: 1.994761e6

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.294e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.922e0

GenotypeQuality
all individuals: 42771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1732
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
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: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: -8.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.091e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 7.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

DP
type: SiteQuality
SIO_000300: 1.994586e6

QD
type: SiteQuality
SIO_000300: 1.327e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2029
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11179
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 9.75e1
variant carriers: 2

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

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

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

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: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.394e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.125e0

FS
type: SiteQuality
SIO_000300: 2.708e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.894e0

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.994537e6

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1700
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 42479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 7.25e1
variant carriers: 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: 16380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001921229586936e-5
allele num: 66624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

DP
type: SiteQuality
SIO_000300: 1.989124e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.319e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1779
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1994
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42251
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 16306
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 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: 6612
num of homozygotes: 0

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

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.0e-4

FS
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MQRankSum
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ReadPosRankSum
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SIO_000300: -9.04e-1

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

South Asian
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allele frequency: 0.0e0
allele num: 16086
num of homozygotes: 0

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

East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

Latino
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allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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QD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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DP
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SIO_000300: 1.936407e6

FS
type: SiteQuality
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VQSLOD
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64968
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 15304
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64960
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East Asian
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African
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allele frequency: 9.924573243350536e-5
allele num: 10076
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Other
type: Population
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QD
type: SiteQuality
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ClippingRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.580128306418481e-5
allele num: 63286
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 61398
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Latino
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Other
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African
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East Asian
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QD
type: SiteQuality
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14236
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.382041e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

QD
type: SiteQuality
SIO_000300: 1.215e1

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

GenotypeQuality
all individuals: 4505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15582
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58000
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.113387395077535e-5
allele num: 14058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.142595978062157e-4
allele num: 8752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

DP
type: SiteQuality
SIO_000300: 1.349699e6

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

FS
type: SiteQuality
SIO_000300: 1.317e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.414e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20763
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.113387395077535e-5
allele num: 14058
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

QD
type: SiteQuality
SIO_000300: 1.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 1.317e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

DP
type: SiteQuality
SIO_000300: 1.349699e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e-1

GenotypeQuality
all individuals: 6976
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 20451
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.64610230737381e-5
allele num: 53134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.222184e6

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

QD
type: SiteQuality
SIO_000300: 1.99e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 1.591e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

GenotypeQuality
all individuals: 4424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 3837
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.879204720562258e-5
allele num: 53214
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.326e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.147e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.148e0

MQRankSum
type: SiteQuality
SIO_000300: -1.271e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.21889e6

QD
type: SiteQuality
SIO_000300: 1.582e1

GenotypeQuality
all individuals: 2017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9529
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7571
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 9.75e1
variant carriers: 27

South Asian
type: Population
allele count: 13
allele frequency: 1.056051990251828e-3
allele num: 12310
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.521220270610976e-4
allele num: 47596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.46611132146914e-5
allele num: 10564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.935458480913026e-4
allele num: 5082
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 1.103594e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.149e1

MQRankSum
type: SiteQuality
SIO_000300: -1.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.082e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.76e-2

GenotypeQuality
all individuals: 586
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.892128565138692e-5
allele num: 40882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.342e-1

DP
type: SiteQuality
SIO_000300: 1.013751e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: -1.333e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

QD
type: SiteQuality
SIO_000300: 1.628e1

GenotypeQuality
all individuals: 8931
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3973
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 195
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variant carriers: 0

GenotypeQuality
all individuals: 1812
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
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GenotypeQuality
all individuals: 2667
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4489
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39146
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.463054187192118e-4
allele num: 4060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.377e0

QD
type: SiteQuality
SIO_000300: 2.366e1

MQ
type: SiteQuality
SIO_000300: 5.336e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: -1.708e0

DP
type: SiteQuality
SIO_000300: 9.94096e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
all individuals: 2381
bin: 3.75e1
variant carriers: 555

GenotypeQuality
all individuals: 2306
bin: 2.75e1
variant carriers: 364

GenotypeQuality
all individuals: 1085
bin: 4.25e1
variant carriers: 455

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 453

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 421

GenotypeQuality
all individuals: 1630
bin: 6.25e1
variant carriers: 562

GenotypeQuality
all individuals: 770
bin: 7.75e1
variant carriers: 633

GenotypeQuality
all individuals: 2834
bin: 1.75e1
variant carriers: 627

GenotypeQuality
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bin: 3.25e1
variant carriers: 506

GenotypeQuality
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bin: 2.25e1
variant carriers: 629

GenotypeQuality
all individuals: 648
bin: 5.75e1
variant carriers: 472

GenotypeQuality
all individuals: 704
bin: 8.25e1
variant carriers: 594

East Asian
type: Population
allele count: 3367
allele frequency: 6.736694677871149e-1
allele num: 4998
num of homozygotes: 1072

Latino
type: Population
allele count: 5468
allele frequency: 5.561432058584215e-1
allele num: 9832
num of homozygotes: 1485

European (Non-Finnish)
type: Population
allele count: 10115
allele frequency: 2.584576860179886e-1
allele num: 39136
num of homozygotes: 1099

European (Finnish)
type: Population
allele count: 1088
allele frequency: 2.814278323848939e-1
allele num: 3866
num of homozygotes: 120

African
type: Population
allele count: 2506
allele frequency: 4.138044914134743e-1
allele num: 6056
num of homozygotes: 467

Other
type: Population
allele count: 198
allele frequency: 3.074534161490683e-1
allele num: 644
num of homozygotes: 26

South Asian
type: Population
allele count: 4126
allele frequency: 3.695807954138302e-1
allele num: 11164
num of homozygotes: 680

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 2.383e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

DP
type: SiteQuality
SIO_000300: 9.68524e5

GenotypeQuality
all individuals: 909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9858
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GenotypeQuality
all individuals: 3312
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3854
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variant carriers: 0

GenotypeQuality
all individuals: 5822
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GenotypeQuality
all individuals: 1542
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GenotypeQuality
all individuals: 1561
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variant carriers: 2

GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 1883
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.722866633992267e-5
allele num: 36726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.834189288334556e-4
allele num: 5452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.48913e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

MQ
type: SiteQuality
SIO_000300: 5.041e1

FS
type: SiteQuality
SIO_000300: 3.015e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.237e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
SIO_000300: 7.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3310
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.711790866688361e-5
allele num: 36876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3722
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

MQ
type: SiteQuality
SIO_000300: 5.097e1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 1.618e1

DP
type: SiteQuality
SIO_000300: 8.47256e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

GenotypeQuality
all individuals: 303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3408
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1965
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13004
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36466
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.42e-1

MQ
type: SiteQuality
SIO_000300: 5.065e1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 8.41756e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.29e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

GenotypeQuality
all individuals: 215
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3823
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5675
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.717834429526553e-5
allele num: 36794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.26863e5

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 5.632e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

FS
type: SiteQuality
SIO_000300: 6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

QD
type: SiteQuality
SIO_000300: 1.916e1

GenotypeQuality
all individuals: 787
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 471
bin: 5.75e1
variant carriers: 12

GenotypeQuality
all individuals: 3823
bin: 1.75e1
variant carriers: 26

GenotypeQuality
all individuals: 3654
bin: 2.75e1
variant carriers: 17

GenotypeQuality
all individuals: 2536
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 393
bin: 7.75e1
variant carriers: 15

GenotypeQuality
all individuals: 4262
bin: 3.75e1
variant carriers: 25

GenotypeQuality
all individuals: 5675
bin: 3.25e1
variant carriers: 23

GenotypeQuality
all individuals: 1666
bin: 4.25e1
variant carriers: 28

GenotypeQuality
all individuals: 3310
bin: 1.25e1
variant carriers: 19

GenotypeQuality
all individuals: 3952
bin: 9.75e1
variant carriers: 2419

GenotypeQuality
all individuals: 312
bin: 7.25e1
variant carriers: 18

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

African
type: Population
allele count: 44
allele frequency: 8.261359369132557e-3
allele num: 5326
num of homozygotes: 0

South Asian
type: Population
allele count: 258
allele frequency: 2.595573440643863e-2
allele num: 9940
num of homozygotes: 6

Other
type: Population
allele count: 16
allele frequency: 2.72108843537415e-2
allele num: 588
num of homozygotes: 0

Latino
type: Population
allele count: 195
allele frequency: 2.111760883690708e-2
allele num: 9234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1682
allele frequency: 4.571397510463662e-2
allele num: 36794
num of homozygotes: 29

European (Finnish)
type: Population
allele count: 60
allele frequency: 1.813784764207981e-2
allele num: 3308
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

MQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

DP
type: SiteQuality
SIO_000300: 8.26863e5

QD
type: SiteQuality
SIO_000300: 1.916e1

MQ
type: SiteQuality
SIO_000300: 5.632e1

GenotypeQuality
all individuals: 739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3351
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33194
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.91131498470948e-4
allele num: 5232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3212
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 6.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 8.19484e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

GenotypeQuality
all individuals: 4237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9991
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 11868
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.807555582334157e-4
allele num: 33194
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.163e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.04e-2

FS
type: SiteQuality
SIO_000300: 6.25e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 8.19484e5

GenotypeQuality
all individuals: 2428
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3963
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.127649977447e-4
allele num: 8868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 8.13629e5

FS
type: SiteQuality
SIO_000300: 5.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.024e-1

MQ
type: SiteQuality
SIO_000300: 6.03e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
all individuals: 778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3963
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2428
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5813
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.852253280091272e-5
allele num: 35060
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.443e1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 8.13629e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.024e-1

FS
type: SiteQuality
SIO_000300: 5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQ
type: SiteQuality
SIO_000300: 6.03e1

GenotypeQuality
all individuals: 1777
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4427
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2443
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 778
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1161
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 5813
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3496
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 3675
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3963
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 412
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 23

Other
type: Population
allele count: 4
allele frequency: 7.042253521126761e-3
allele num: 568
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.192168546499255e-4
allele num: 9398
num of homozygotes: 0

Latino
type: Population
allele count: 49
allele frequency: 5.525484889490302e-3
allele num: 8868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

African
type: Population
allele count: 390
allele frequency: 7.166482910694598e-2
allele num: 5442
num of homozygotes: 9

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 1.483171705647461e-3
allele num: 35060
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.024e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 8.13629e5

MQ
type: SiteQuality
SIO_000300: 6.03e1

FS
type: SiteQuality
SIO_000300: 5.85e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 207
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3496
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2070
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35060
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.512679162072767e-4
allele num: 5442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 8.13629e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.03e1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.024e-1

GenotypeQuality
all individuals: 946
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.712e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

DP
type: SiteQuality
SIO_000300: 3.939569e6

GenotypeQuality
all individuals: 1160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 8.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.104e0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

DP
type: SiteQuality
SIO_000300: 3.94012e6

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49277
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 963
bin: 8.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
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

DP
type: SiteQuality
SIO_000300: 3.941197e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.618e1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 1.453e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeQuality
all individuals: 374
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
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: 10404
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.649e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.551e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

DP
type: SiteQuality
SIO_000300: 3.946054e6

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49280
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

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

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

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

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: 16388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.68e0

QD
type: SiteQuality
SIO_000300: 2.287e1

FS
type: SiteQuality
SIO_000300: 4.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

DP
type: SiteQuality
SIO_000300: 3.959127e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -2.892e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

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

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
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GenotypeQuality
all individuals: 987
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49317
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 5180
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 52
allele frequency: 3.162632283177229e-3
allele num: 16442
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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.099580083983203e-4
allele num: 66680
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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.675e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

DP
type: SiteQuality
SIO_000300: 3.96478e6

QD
type: SiteQuality
SIO_000300: 1.78e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

GenotypeQuality
all individuals: 1006
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 595
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variant carriers: 0

GenotypeQuality
all individuals: 5228
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.75e1
variant carriers: 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: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.386e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

DP
type: SiteQuality
SIO_000300: 3.963593e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.11e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49297
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
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

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
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: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 3.966444e6

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.557e0

VQSLOD
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ClippingRankSum
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SIO_000300: -5.33e-1

QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.249212775528565e-4
allele num: 66690
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Latino
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MQ
type: SiteQuality
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 6.933210076265311e-4
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

Other
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South Asian
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African
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East Asian
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.99805126667666e-5
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East Asian
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South Asian
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Latino
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Other
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VQSLOD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele count: 1
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allele num: 66710
num of homozygotes: 0

Other
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DP
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InbreedingCoeff
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FS
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MQ
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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FS
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 66718
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MQRankSum
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QD
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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South Asian
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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South Asian
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European (Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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African
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European (Non-Finnish)
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East Asian
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South Asian
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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FS
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MQRankSum
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Other
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Latino
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African
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East Asian
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European (Finnish)
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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European (Finnish)
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South Asian
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QD
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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DP
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VQSLOD
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MQ
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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allele num: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

DP
type: SiteQuality
SIO_000300: 3.985115e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.236e1

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
all individuals: 613
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1008
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2199e1

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

DP
type: SiteQuality
SIO_000300: 3.966126e6

VQSLOD
type: SiteQuality
SIO_000300: -9.123e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.882e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.03e-1

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1008
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49268
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1496
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 7.75e1
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

African
type: Population
allele count: 8
allele frequency: 7.68787238131847e-4
allele num: 10406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.966793e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

GenotypeQuality
all individuals: 4540
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1114
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1242
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 483
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 8.75e1
variant carriers: 1

African
type: Population
allele count: 339
allele frequency: 3.257735921583702e-2
allele num: 10406
num of homozygotes: 2

Other
type: Population
allele count: 141
allele frequency: 1.552863436123348e-1
allele num: 908
num of homozygotes: 17

European (Finnish)
type: Population
allele count: 1769
allele frequency: 2.674629573631691e-1
allele num: 6614
num of homozygotes: 256

East Asian
type: Population
allele count: 1490
allele frequency: 1.722543352601156e-1
allele num: 8650
num of homozygotes: 135

Latino
type: Population
allele count: 795
allele frequency: 6.866470893073069e-2
allele num: 11578
num of homozygotes: 29

European (Non-Finnish)
type: Population
allele count: 10588
allele frequency: 1.58669264199011e-1
allele num: 66730
num of homozygotes: 856

South Asian
type: Population
allele count: 2528
allele frequency: 1.531193216232586e-1
allele num: 16510
num of homozygotes: 208

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.684e1

DP
type: SiteQuality
SIO_000300: 5.601692e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.171e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 7147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 138
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42912
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
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: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 1.338e0

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.267e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 4.257134e6

GenotypeQuality
all individuals: 983
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6780
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42911
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1037
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
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

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.145e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

FS
type: SiteQuality
SIO_000300: 1.681e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

DP
type: SiteQuality
SIO_000300: 4.250405e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.391e1

GenotypeQuality
all individuals: 1844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1037
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
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: 16460
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.957713390759593e-4
allele num: 10216
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: -3.858e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 4.250344e6

FS
type: SiteQuality
SIO_000300: 2.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

GenotypeQuality
all individuals: 1844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 983
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.215066828675577e-4
allele num: 16460
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

MQ
type: SiteQuality
SIO_000300: 5.759e1

DP
type: SiteQuality
SIO_000300: 4.250329e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 2.285e0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

QD
type: SiteQuality
SIO_000300: 1.661e1

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1