11-64055270-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055270
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055270
    reference: chr 11
allele count: 14
allele frequency: 1.169903399405021e-4
allele num: 119668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.485A>G
  hgvsp: ENSP00000321698.3:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.485A>G
  hgvsp: ENSP00000445000.1:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.485A>G
  hgvsp: ENSP00000438716.1:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-542A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-112A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.659A>G
  hgvsp: ENSP00000411827.1:p.His220Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.485A>G
  hgvsp: ENSP00000441003.1:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.485A>G
  hgvsp: ENSP00000415698.2:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.503A>G
  hgvsp: ENSP00000445570.1:p.His168Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.485A>G
  hgvsp: ENSP00000442792.1:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.485A>G
  hgvsp: ENSP00000366931.4:p.His162Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.900A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-197A>G
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His220Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

11-64055278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055278
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055278
    reference: chr 11
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.493C>T
  hgvsp: ENSP00000445000.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.511C>T
  hgvsp: ENSP00000445570.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.667C>T
  hgvsp: ENSP00000411827.1:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.493C>T
  hgvsp: ENSP00000366931.4:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.493C>T
  hgvsp: ENSP00000442792.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-534C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-189C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.493C>T
  hgvsp: ENSP00000415698.2:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.493C>T
  hgvsp: ENSP00000321698.3:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.493C>T
  hgvsp: ENSP00000441003.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.493C>T
  hgvsp: ENSP00000438716.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.908C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-104C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg223Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

11-64055279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055279
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055279
    reference: chr 11
allele count: 7
allele frequency: 5.845023380093521e-5
allele num: 119760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.512G>A
  hgvsp: ENSP00000445570.1:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.909G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.494G>A
  hgvsp: ENSP00000366931.4:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.668G>A
  hgvsp: ENSP00000411827.1:p.Arg223Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.494G>A
  hgvsp: ENSP00000445000.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.494G>A
  hgvsp: ENSP00000438716.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.494G>A
  hgvsp: ENSP00000441003.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-103G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.494G>A
  hgvsp: ENSP00000321698.3:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.494G>A
  hgvsp: ENSP00000442792.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-533G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-188G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.494G>A
  hgvsp: ENSP00000415698.2:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg223Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

11-64055283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055283
    reference: chr 11
allele count: 1
allele frequency: 8.347663488989432e-6
allele num: 119794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.498A>G
  hgvsp: ENST00000539851.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.498A>G
  hgvsp: ENST00000543383.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.498A>G
  hgvsp: ENST00000538032.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.498A>G
  hgvsp: ENST00000377702.4:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.498A>G
  hgvsp: ENST00000438980.2:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-99A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-529A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.516A>G
  hgvsp: ENST00000546139.1:c.516A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-184A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.498A>G
  hgvsp: ENST00000539833.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.672A>G
  hgvsp: ENST00000411458.1:c.672A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.913A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.498A>G
  hgvsp: ENST00000313074.3:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala224Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-64055285-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055285
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055285
    reference: chr 11
allele count: 1
allele frequency: 8.346966712296751e-6
allele num: 119804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.500A>G
  hgvsp: ENSP00000321698.3:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.518A>G
  hgvsp: ENSP00000445570.1:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.915A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-182A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.500A>G
  hgvsp: ENSP00000441003.1:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.500A>G
  hgvsp: ENSP00000445000.1:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-97A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.500A>G
  hgvsp: ENSP00000442792.1:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.500A>G
  hgvsp: ENSP00000366931.4:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.500A>G
  hgvsp: ENSP00000438716.1:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-527A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.674A>G
  hgvsp: ENSP00000411827.1:p.Gln225Arg
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.500A>G
  hgvsp: ENSP00000415698.2:p.Gln167Arg
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln225Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

11-64055286-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055286
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055286
    reference: chr 11
allele count: 2
allele frequency: 1.669783596045953e-5
allele num: 119776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-96G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-181G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.916G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.501G>C
  hgvsp: ENSP00000441003.1:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-526G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.501G>C
  hgvsp: ENSP00000442792.1:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.519G>C
  hgvsp: ENSP00000445570.1:p.Gln173His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445000
  ensembl transcript: ENST00000538032
  gene symbol: GPR137
  hgvsc: ENST00000538032.1:c.501G>C
  hgvsp: ENSP00000445000.1:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.501G>C
  hgvsp: ENSP00000321698.3:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.501G>C
  hgvsp: ENSP00000415698.2:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.501G>C
  hgvsp: ENSP00000438716.1:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.675G>C
  hgvsp: ENSP00000411827.1:p.Gln225His
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.501G>C
  hgvsp: ENSP00000366931.4:p.Gln167His
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln225His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

11-64055295-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055295
    reference: chr 11
allele count: 2
allele frequency: 1.669281874937402e-5
allele num: 119812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.528C>G
  hgvsp: ENST00000546139.1:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.510C>G
  hgvsp: ENST00000543383.1:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-517C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.510C>G
  hgvsp: ENST00000539851.1:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.684C>G
  hgvsp: ENST00000411458.1:c.684C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.510C>G
  hgvsp: ENST00000313074.3:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.510C>G
  hgvsp: ENST00000377702.4:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.510C>G
  hgvsp: ENST00000539833.1:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.510C>G
  hgvsp: ENST00000438980.2:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-87C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.925C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-172C>G
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala228Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

11-64055302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055302
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055302
    reference: chr 11
allele count: 4
allele frequency: 3.338730948366526e-5
allele num: 119806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.517C>T
  hgvsp: ENSP00000366931.4:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-165C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-80C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.691C>T
  hgvsp: ENSP00000411827.1:p.Leu231Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.517C>T
  hgvsp: ENSP00000441003.1:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-510C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.517C>T
  hgvsp: ENSP00000438716.1:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.517C>T
  hgvsp: ENSP00000321698.3:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.517C>T
  hgvsp: ENSP00000442792.1:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.517C>T
  hgvsp: ENSP00000415698.2:p.Leu173Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.535C>T
  hgvsp: ENSP00000445570.1:p.Leu179Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.932C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu231Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-64055308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055308
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055308
    reference: chr 11
allele count: 2
allele frequency: 1.669532697797886e-5
allele num: 119794
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.697C>T
  hgvsp: ENSP00000411827.1:p.Arg233Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.523C>T
  hgvsp: ENSP00000366931.4:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-159C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.523C>T
  hgvsp: ENSP00000321698.3:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.523C>T
  hgvsp: ENSP00000438716.1:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.523C>T
  hgvsp: ENSP00000441003.1:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.523C>T
  hgvsp: ENSP00000415698.2:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.523C>T
  hgvsp: ENSP00000442792.1:p.Arg175Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.541C>T
  hgvsp: ENSP00000445570.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-504C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-74C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.938C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg233Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

11-64055311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055311
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055311
    reference: chr 11
allele count: 1
allele frequency: 8.347245409015026e-6
allele num: 119800
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.700G>A
  hgvsp: ENSP00000411827.1:p.Val234Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-71G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.526G>A
  hgvsp: ENSP00000442792.1:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-156G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.526G>A
  hgvsp: ENSP00000366931.4:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.526G>A
  hgvsp: ENSP00000321698.3:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.526G>A
  hgvsp: ENSP00000441003.1:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.526G>A
  hgvsp: ENSP00000415698.2:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.526G>A
  hgvsp: ENSP00000438716.1:p.Val176Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-501G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.941G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.544G>A
  hgvsp: ENSP00000445570.1:p.Val182Ile
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8451
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val234Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

11-64055322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055322
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055322
    reference: chr 11
allele count: 2
allele frequency: 1.670118244371702e-5
allele num: 119752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.537C>T
  hgvsp: ENST00000438980.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.537C>T
  hgvsp: ENST00000539833.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.952C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-490C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.555C>T
  hgvsp: ENST00000546139.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-145C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.711C>T
  hgvsp: ENST00000411458.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-60C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.537C>T
  hgvsp: ENST00000543383.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.537C>T
  hgvsp: ENST00000313074.3:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.537C>T
  hgvsp: ENST00000539851.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.537C>T
  hgvsp: ENST00000377702.4:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser237Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

11-64055328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055328
    reference: chr 11
allele count: 1
allele frequency: 8.349336227769892e-6
allele num: 119770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.543C>T
  hgvsp: ENST00000539851.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.958C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.561C>T
  hgvsp: ENST00000546139.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-484C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.543C>T
  hgvsp: ENST00000543383.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.543C>T
  hgvsp: ENST00000377702.4:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-139C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.543C>T
  hgvsp: ENST00000438980.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.543C>T
  hgvsp: ENST00000539833.1:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.717C>T
  hgvsp: ENST00000411458.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.543C>T
  hgvsp: ENST00000313074.3:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-54C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser239Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

11-64055331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055331
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055331
    reference: chr 11
allele count: 1
allele frequency: 8.351009637065121e-6
allele num: 119746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-481G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-51G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.720G>A
  hgvsp: ENST00000411458.1:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.961G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.546G>A
  hgvsp: ENST00000539833.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.546G>A
  hgvsp: ENST00000539851.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.564G>A
  hgvsp: ENST00000546139.1:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.546G>A
  hgvsp: ENST00000377702.4:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.546G>A
  hgvsp: ENST00000313074.3:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.546G>A
  hgvsp: ENST00000543383.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-136G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.546G>A
  hgvsp: ENST00000438980.2:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu240Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-64055334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055334
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055334
    reference: chr 11
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-133C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.567C>T
  hgvsp: ENST00000546139.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-478C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.549C>T
  hgvsp: ENST00000543383.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.549C>T
  hgvsp: ENST00000438980.2:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.549C>T
  hgvsp: ENST00000313074.3:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.549C>T
  hgvsp: ENST00000539833.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.549C>T
  hgvsp: ENST00000377702.4:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.549C>T
  hgvsp: ENST00000539851.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.964C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.723C>T
  hgvsp: ENST00000411458.1:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-48C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe241Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-64055335-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055335
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055335
    reference: chr 11
allele count: 5
allele frequency: 4.177528240090903e-5
allele num: 119688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-47G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.965G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.724G>T
  hgvsp: ENSP00000411827.1:p.Val242Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.550G>T
  hgvsp: ENSP00000442792.1:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-132G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-477G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.550G>T
  hgvsp: ENSP00000415698.2:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.550G>T
  hgvsp: ENSP00000366931.4:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.550G>T
  hgvsp: ENSP00000441003.1:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.550G>T
  hgvsp: ENSP00000321698.3:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.568G>T
  hgvsp: ENSP00000445570.1:p.Val190Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.550G>T
  hgvsp: ENSP00000438716.1:p.Val184Phe
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10469
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val242Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

11-64055343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055343
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055343
    reference: chr 11
allele count: 11
allele frequency: 9.197785842099102e-5
allele num: 119594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.558C>T
  hgvsp: ENST00000438980.2:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.558C>T
  hgvsp: ENST00000377702.4:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.558C>T
  hgvsp: ENST00000543383.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-39C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.973C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.558C>T
  hgvsp: ENST00000539851.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.558C>T
  hgvsp: ENST00000313074.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-469C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.732C>T
  hgvsp: ENST00000411458.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.558C>T
  hgvsp: ENST00000539833.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-124C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.576C>T
  hgvsp: ENST00000546139.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Cys244Cys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-64055344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055344
    reference: chr 11
allele count: 1
allele frequency: 8.362182864214875e-6
allele num: 119586
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.733G>A
  hgvsp: ENSP00000411827.1:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.559G>A
  hgvsp: ENSP00000441003.1:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.559G>A
  hgvsp: ENSP00000366931.4:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.577G>A
  hgvsp: ENSP00000445570.1:p.Ala193Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.559G>A
  hgvsp: ENSP00000442792.1:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.559G>A
  hgvsp: ENSP00000415698.2:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-38G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.559G>A
  hgvsp: ENSP00000438716.1:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-123G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.559G>A
  hgvsp: ENSP00000321698.3:p.Ala187Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-468G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.974G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala245Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-64055347-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055347
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055345
    reference: chr 11
allele count: 1
allele frequency: 8.369601606963508e-6
allele num: 119480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.564_565delGT
  hgvsp: ENSP00000441003.1:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.564_565delGT
  hgvsp: ENSP00000366931.4:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-463_408-462delGT
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-33_408-32delGT
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.979_980delGT
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.564_565delGT
  hgvsp: ENSP00000415698.2:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.582_583delGT
  hgvsp: ENSP00000445570.1:p.Leu196CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.564_565delGT
  hgvsp: ENSP00000321698.3:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.564_565delGT
  hgvsp: ENSP00000442792.1:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-118_408-117delGT
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.564_565delGT
  hgvsp: ENSP00000438716.1:p.Leu190CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.738_739delGT
  hgvsp: ENSP00000411827.1:p.Leu248CysfsTer15
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu248CysfsTer15
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: CTG
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

11-64055348-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055348
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055348
    reference: chr 11
allele count: 1
allele frequency: 8.36946150884652e-6
allele num: 119482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-119T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.563T>C
  hgvsp: ENSP00000415698.2:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.563T>C
  hgvsp: ENSP00000441003.1:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.563T>C
  hgvsp: ENSP00000321698.3:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-464T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-34T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.563T>C
  hgvsp: ENSP00000366931.4:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.978T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.563T>C
  hgvsp: ENSP00000438716.1:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.563T>C
  hgvsp: ENSP00000442792.1:p.Leu188Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.581T>C
  hgvsp: ENSP00000445570.1:p.Leu194Pro
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.737T>C
  hgvsp: ENSP00000411827.1:p.Leu246Pro
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu246Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

11-64055365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055365
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055365
    reference: chr 11
allele count: 8
allele frequency: 6.716706127315165e-5
allele num: 119106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.580C>T
  hgvsp: ENSP00000442792.1:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.598C>T
  hgvsp: ENSP00000445570.1:p.Leu200Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.580C>T
  hgvsp: ENSP00000321698.3:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-447C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.580C>T
  hgvsp: ENSP00000366931.4:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.580C>T
  hgvsp: ENSP00000438716.1:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.995C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.580C>T
  hgvsp: ENSP00000441003.1:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.580C>T
  hgvsp: ENSP00000415698.2:p.Leu194Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-102C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-17C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.754C>T
  hgvsp: ENSP00000411827.1:p.Leu252Phe
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu252Phe
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-64055369-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055369
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055369
    reference: chr 11
allele count: 2
allele frequency: 1.682340472064736e-5
allele num: 118882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.602G>T
  hgvsp: ENSP00000445570.1:p.Cys201Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.758G>T
  hgvsp: ENSP00000411827.1:p.Cys253Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.999G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.584G>T
  hgvsp: ENSP00000321698.3:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.584G>T
  hgvsp: ENSP00000438716.1:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.584G>T
  hgvsp: ENSP00000442792.1:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-13G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.584G>T
  hgvsp: ENSP00000441003.1:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.584G>T
  hgvsp: ENSP00000366931.4:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.584G>T
  hgvsp: ENSP00000415698.2:p.Cys195Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-98G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-443G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys253Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-64055373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055373
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055373
    reference: chr 11
allele count: 19
allele frequency: 1.603104961187985e-4
allele num: 118520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.588C>T
  hgvsp: ENST00000539851.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.588C>T
  hgvsp: ENST00000543383.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.606C>T
  hgvsp: ENST00000546139.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.588C>T
  hgvsp: ENST00000313074.3:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1003C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-94C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-9C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-439C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.588C>T
  hgvsp: ENST00000539833.1:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.588C>T
  hgvsp: ENST00000377702.4:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.588C>T
  hgvsp: ENST00000438980.2:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.762C>T
  hgvsp: ENST00000411458.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8420
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu254Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

11-64055374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055374
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055374
    reference: chr 11
allele count: 1
allele frequency: 8.434547908232118e-6
allele num: 118560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.589G>A
  hgvsp: ENSP00000441003.1:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.589G>A
  hgvsp: ENSP00000438716.1:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.589G>A
  hgvsp: ENSP00000415698.2:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.589G>A
  hgvsp: ENSP00000442792.1:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-8G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1004G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.607G>A
  hgvsp: ENSP00000445570.1:p.Val203Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-438G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.589G>A
  hgvsp: ENSP00000321698.3:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-93G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.763G>A
  hgvsp: ENSP00000411827.1:p.Val255Ile
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.589G>A
  hgvsp: ENSP00000366931.4:p.Val197Ile
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val255Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/11-64055376-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055376
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055376
    reference: chr 11
allele count: 3
allele frequency: 2.531132935101752e-5
allele num: 118524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.609C>A
  hgvsp: ENST00000546139.1:c.609C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.591C>A
  hgvsp: ENST00000377702.4:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.765C>A
  hgvsp: ENST00000411458.1:c.765C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.591C>A
  hgvsp: ENST00000543383.1:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.591C>A
  hgvsp: ENST00000539833.1:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1006C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-436C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.591C>A
  hgvsp: ENST00000539851.1:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-6C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.591C>A
  hgvsp: ENST00000438980.2:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-91C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.591C>A
  hgvsp: ENST00000313074.3:c.591C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-6C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-64055376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055376
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055376
    reference: chr 11
allele count: 2
allele frequency: 1.687421956734501e-5
allele num: 118524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.591C>T
  hgvsp: ENST00000438980.2:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-91C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.609C>T
  hgvsp: ENST00000546139.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.591C>T
  hgvsp: ENST00000539833.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-6C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.591C>T
  hgvsp: ENST00000543383.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.765C>T
  hgvsp: ENST00000411458.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.591C>T
  hgvsp: ENST00000539851.1:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.591C>T
  hgvsp: ENST00000313074.3:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-436C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.591C>T
  hgvsp: ENST00000377702.4:c.591C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1006C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-6C>T
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

11-64055377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055377
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055377
    reference: chr 11
allele count: 9
allele frequency: 7.628282280347849e-5
allele num: 117982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-90G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.592G>A
  hgvsp: ENSP00000441003.1:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.766G>A
  hgvsp: ENSP00000411827.1:p.Ala256Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1007G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-5G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.592G>A
  hgvsp: ENSP00000366931.4:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.592G>A
  hgvsp: ENSP00000438716.1:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.592G>A
  hgvsp: ENSP00000415698.2:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.592G>A
  hgvsp: ENSP00000442792.1:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.592G>A
  hgvsp: ENSP00000321698.3:p.Ala198Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.610G>A
  hgvsp: ENSP00000445570.1:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-435G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala256Thr
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-64055380-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055380
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055380
    reference: chr 11
allele count: 4
allele frequency: 3.39172757644106e-5
allele num: 117934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1010A>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.595A>C
  hgvsp: ENST00000539833.1:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.595A>C
  hgvsp: ENST00000377702.4:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.595A>C
  hgvsp: ENST00000438980.2:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.769A>C
  hgvsp: ENST00000411458.1:c.769A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-432A>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.595A>C
  hgvsp: ENST00000313074.3:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.595A>C
  hgvsp: ENST00000539851.1:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.595A>C
  hgvsp: ENST00000543383.1:c.595A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.408-2A>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.613A>C
  hgvsp: ENST00000546139.1:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-87A>C
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9863
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-2A>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

11-64055384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055384
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055384
    reference: chr 11
allele count: 5
allele frequency: 4.247727465805794e-5
allele num: 117710
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.773G>A
  hgvsp: ENSP00000411827.1:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1014G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.410G>A
  hgvsp: ENSP00000442929.1:p.Arg137Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.599G>A
  hgvsp: ENSP00000366931.4:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.599G>A
  hgvsp: ENSP00000441003.1:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.599G>A
  hgvsp: ENSP00000321698.3:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-428G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.617G>A
  hgvsp: ENSP00000445570.1:p.Arg206Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.599G>A
  hgvsp: ENSP00000442792.1:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.599G>A
  hgvsp: ENSP00000438716.1:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-83G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.599G>A
  hgvsp: ENSP00000415698.2:p.Arg200Gln
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg258Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

11-64055385-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055385
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055385
    reference: chr 11
allele count: 2
allele frequency: 1.69848495142333e-5
allele num: 117752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-427G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.600G>C
  hgvsp: ENST00000377702.4:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.600G>C
  hgvsp: ENST00000539851.1:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.600G>C
  hgvsp: ENST00000313074.3:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.618G>C
  hgvsp: ENST00000546139.1:c.618G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.411G>C
  hgvsp: ENST00000541952.1:c.411G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.600G>C
  hgvsp: ENST00000438980.2:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.600G>C
  hgvsp: ENST00000543383.1:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1015G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-82G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.600G>C
  hgvsp: ENST00000539833.1:c.600G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.774G>C
  hgvsp: ENST00000411458.1:c.774G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8353
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg258Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-64055387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055387
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055387
    reference: chr 11
allele count: 2
allele frequency: 1.700738120344229e-5
allele num: 117596
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.413C>T
  hgvsp: ENSP00000442929.1:p.Ala138Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.602C>T
  hgvsp: ENSP00000441003.1:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-425C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.602C>T
  hgvsp: ENSP00000366931.4:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.776C>T
  hgvsp: ENSP00000411827.1:p.Ala259Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-80C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.602C>T
  hgvsp: ENSP00000442792.1:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.602C>T
  hgvsp: ENSP00000415698.2:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.620C>T
  hgvsp: ENSP00000445570.1:p.Ala207Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.602C>T
  hgvsp: ENSP00000321698.3:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.602C>T
  hgvsp: ENSP00000438716.1:p.Ala201Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1017C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala259Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-64055388-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055388
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055388
    reference: chr 11
allele count: 88
allele frequency: 7.499701716409007e-4
allele num: 117338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.603G>T
  hgvsp: ENST00000539833.1:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.603G>T
  hgvsp: ENST00000313074.3:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.777G>T
  hgvsp: ENST00000411458.1:c.777G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.414G>T
  hgvsp: ENST00000541952.1:c.414G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.603G>T
  hgvsp: ENST00000438980.2:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.603G>T
  hgvsp: ENST00000377702.4:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.621G>T
  hgvsp: ENST00000546139.1:c.621G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1018G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.603G>T
  hgvsp: ENST00000539851.1:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.603G>T
  hgvsp: ENST00000543383.1:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-79G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-424G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala259Ala
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

11-64055388-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055388
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055388
    reference: chr 11
allele count: 2
allele frequency: 1.704477662820229e-5
allele num: 117338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.414G>A
  hgvsp: ENST00000541952.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.621G>A
  hgvsp: ENST00000546139.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.603G>A
  hgvsp: ENST00000543383.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1018G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.603G>A
  hgvsp: ENST00000539851.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.603G>A
  hgvsp: ENST00000438980.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.777G>A
  hgvsp: ENST00000411458.1:c.777G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-79G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.603G>A
  hgvsp: ENST00000313074.3:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-424G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.603G>A
  hgvsp: ENST00000539833.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.603G>A
  hgvsp: ENST00000377702.4:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala259Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-64055391-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055391
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055391
    reference: chr 11
allele count: 5
allele frequency: 4.234847714876173e-5
allele num: 118068
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.606C>G
  hgvsp: ENST00000313074.3:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.780C>G
  hgvsp: ENST00000411458.1:c.780C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.606C>G
  hgvsp: ENST00000377702.4:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.417C>G
  hgvsp: ENST00000541952.1:c.417C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.606C>G
  hgvsp: ENST00000438980.2:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-421C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.606C>G
  hgvsp: ENST00000539851.1:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.606C>G
  hgvsp: ENST00000543383.1:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.624C>G
  hgvsp: ENST00000546139.1:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.606C>G
  hgvsp: ENST00000539833.1:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1021C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-76C>G
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6887
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11102
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro260Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

11-64055391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055391
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055391
    reference: chr 11
allele count: 6
allele frequency: 5.081817257851407e-5
allele num: 118068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.606C>T
  hgvsp: ENST00000543383.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.606C>T
  hgvsp: ENST00000539851.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-421C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.606C>T
  hgvsp: ENST00000377702.4:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.606C>T
  hgvsp: ENST00000313074.3:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1021C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.606C>T
  hgvsp: ENST00000539833.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-76C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.780C>T
  hgvsp: ENST00000411458.1:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.606C>T
  hgvsp: ENST00000438980.2:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.417C>T
  hgvsp: ENST00000541952.1:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.624C>T
  hgvsp: ENST00000546139.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro260Pro
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-64055397-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055397
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055397
    reference: chr 11
allele count: 1
allele frequency: 8.469838903664053e-6
allele num: 118066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.630T>C
  hgvsp: ENST00000546139.1:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.612T>C
  hgvsp: ENST00000539851.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.786T>C
  hgvsp: ENST00000411458.1:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-415T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.612T>C
  hgvsp: ENST00000543383.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.612T>C
  hgvsp: ENST00000438980.2:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.423T>C
  hgvsp: ENST00000541952.1:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1027T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-70T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.612T>C
  hgvsp: ENST00000377702.4:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.612T>C
  hgvsp: ENST00000539833.1:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.612T>C
  hgvsp: ENST00000313074.3:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr262Thr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

11-64055413-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055413
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055413
    reference: chr 11
allele count: 2
allele frequency: 1.694829076487636e-5
allele num: 118006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1043G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.802G>A
  hgvsp: ENSP00000411827.1:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.628G>A
  hgvsp: ENSP00000366931.4:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-399G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.646G>A
  hgvsp: ENSP00000445570.1:p.Ala216Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.628G>A
  hgvsp: ENSP00000441003.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.628G>A
  hgvsp: ENSP00000321698.3:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.628G>A
  hgvsp: ENSP00000415698.2:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.628G>A
  hgvsp: ENSP00000442792.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.439G>A
  hgvsp: ENSP00000442929.1:p.Ala147Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.628G>A
  hgvsp: ENSP00000438716.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala268Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-64055413-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055413
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055413
    reference: chr 11
allele count: 1
allele frequency: 8.474145382438182e-6
allele num: 118006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.628G>T
  hgvsp: ENSP00000415698.2:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.628G>T
  hgvsp: ENSP00000441003.1:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.802G>T
  hgvsp: ENSP00000411827.1:p.Ala268Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.628G>T
  hgvsp: ENSP00000321698.3:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.628G>T
  hgvsp: ENSP00000366931.4:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.628G>T
  hgvsp: ENSP00000438716.1:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-54G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.628G>T
  hgvsp: ENSP00000442792.1:p.Ala210Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.439G>T
  hgvsp: ENSP00000442929.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.646G>T
  hgvsp: ENSP00000445570.1:p.Ala216Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1043G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-399G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala268Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

11-64055425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055425
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055425
    reference: chr 11
allele count: 2
allele frequency: 1.693566142225685e-5
allele num: 118094
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1055C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+7C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-42C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-387C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+7C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.807+7C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-64055439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055439
    reference: chr 11
allele count: 1
allele frequency: 8.480613317955154e-6
allele num: 117916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1069C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-28C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-373C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+21C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-64055441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055441
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055441
    reference: chr 11
allele count: 2
allele frequency: 1.696496734243787e-5
allele num: 117890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-371C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1071C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+23C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-26C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-64055454-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055454
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055454
    reference: chr 11
allele count: 22
allele frequency: 1.868650834097781e-4
allele num: 117732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-13G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1084G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-358G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+36G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10148
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-64055461-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055461
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055461
    reference: chr 11
allele count: 16
allele frequency: 1.362653085557581e-4
allele num: 117418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1091C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-6C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-351C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+43C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+43C>A
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-6C>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

11-64055461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055461
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055461
    reference: chr 11
allele count: 3
allele frequency: 2.554974535420464e-5
allele num: 117418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-351C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-6C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1091C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+43C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-6C>T
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-64055462-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055462
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055462
    reference: chr 11
allele count: 3
allele frequency: 2.554974535420464e-5
allele num: 117418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408-5G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1092G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+44G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-350G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+44G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408-5G>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

11-64055467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055467
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055467
    reference: chr 11
allele count: 2
allele frequency: 1.704041987594574e-5
allele num: 117368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-345C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.408C>T
  hgvsp: ENST00000542190.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+49C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1097C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+49C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.408C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

11-64055468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055468
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055468
    reference: chr 11
allele count: 1
allele frequency: 8.522678848415634e-6
allele num: 117334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.409G>A
  hgvsp: ENSP00000441034.1:p.Gly137Ser
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1098G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+50G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-344G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly137Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

11-64055472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055472
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055472
    reference: chr 11
allele count: 1
allele frequency: 8.517887563884156e-6
allele num: 117400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.413C>T
  hgvsp: ENSP00000441034.1:p.Ser138Phe
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-340C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1102C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+54C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser138Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-64055475-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055475
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055475
    reference: chr 11
allele count: 1
allele frequency: 8.519919571959241e-6
allele num: 117372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.444+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1105A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441034
  ensembl transcript: ENST00000542190
  gene symbol: GPR137
  hgvsc: ENST00000542190.1:c.416A>T
  hgvsp: ENSP00000441034.1:p.Gln139Leu
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.807+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-337A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.633+57A>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.651+57A>T
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln139Leu
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: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

11-64055480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055480
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055480
    reference: chr 11
allele count: 1
allele frequency: 8.515711487694797e-6
allele num: 117430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+62G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1110G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-332G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-57G>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-57G>C
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

11-64055483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055483
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055483
    reference: chr 11
allele count: 1
allele frequency: 8.51368148614824e-6
allele num: 117458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-329G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000536017
  gene symbol: GPR137
  hgvsc: ENST00000536017.1:n.1113G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+65G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-54G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-54G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

11-64055496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055496
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055496
    reference: chr 11
allele count: 2
allele frequency: 1.700535668735652e-5
allele num: 117610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+78G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-316G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-41G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-41G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20807
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-64055497-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055497
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055497
    reference: chr 11
allele count: 32
allele frequency: 2.720810801618882e-4
allele num: 117612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-315C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+79C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-40C>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-40C>A
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-64055501-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055501
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055501
    reference: chr 11
allele count: 2
allele frequency: 1.699235344095157e-5
allele num: 117700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+83C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-36C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-311C>G
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-64055507-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055507
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055507
    reference: chr 11
allele count: 1
allele frequency: 8.496321092966746e-6
allele num: 117698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-305C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+89C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-30C>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-30C>G
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3991
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-64055507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055507
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055507
    reference: chr 11
allele count: 1
allele frequency: 8.496321092966746e-6
allele num: 117698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-305C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+89C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-30C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-30C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-64055513-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055513
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055513
    reference: chr 11
allele count: 1
allele frequency: 8.484066922319883e-6
allele num: 117868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+95G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-299G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-24G>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-24G>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11209
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

11-64055518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055518
    reference: chr 11
allele count: 5
allele frequency: 4.241025989007261e-5
allele num: 117896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+100C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-294C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-19C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-19C>T
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12911
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-64055525-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055525
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055525
    reference: chr 11
allele count: 1
allele frequency: 8.471560969824299e-6
allele num: 118042
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.808-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.445-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.634-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+107T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.634-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-287T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.634-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.634-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.634-12T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.652-12T>C
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3995
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-64055556-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055556
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055556
    reference: chr 11
allele count: 3
allele frequency: 2.526996748597517e-5
allele num: 118718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+138C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.653C>T
  hgvsp: ENSP00000438716.1:p.Ala218Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.653C>T
  hgvsp: ENSP00000442792.1:p.Ala218Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.827C>T
  hgvsp: ENSP00000411827.1:p.Ala276Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-256C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.653C>T
  hgvsp: ENSP00000321698.3:p.Ala218Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.653C>T
  hgvsp: ENSP00000441003.1:p.Ala218Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.2C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.671C>T
  hgvsp: ENSP00000445570.1:p.Ala224Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.653C>T
  hgvsp: ENSP00000415698.2:p.Ala218Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.464C>T
  hgvsp: ENSP00000442929.1:p.Ala155Val
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala276Val
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

11-64055557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055557
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055557
    reference: chr 11
allele count: 62
allele frequency: 5.214641367245323e-4
allele num: 118896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+139G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.654G>A
  hgvsp: ENST00000438980.2:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.654G>A
  hgvsp: ENST00000539851.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.3G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-255G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.828G>A
  hgvsp: ENST00000411458.1:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.672G>A
  hgvsp: ENST00000546139.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.654G>A
  hgvsp: ENST00000539833.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.465G>A
  hgvsp: ENST00000541952.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.654G>A
  hgvsp: ENST00000543383.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.654G>A
  hgvsp: ENST00000313074.3:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Ala276Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

11-64055561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055561
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055561
    reference: chr 11
allele count: 5
allele frequency: 4.201610056973833e-5
allele num: 119002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.676G>A
  hgvsp: ENST00000546139.1:c.676G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.658G>A
  hgvsp: ENSP00000441003.1:p.Ala220Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.658G>A
  hgvsp: ENST00000539833.1:c.658G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+143G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442929
  ensembl transcript: ENST00000541952
  gene symbol: GPR137
  hgvsc: ENST00000541952.1:c.469G>A
  hgvsp: ENST00000541952.1:c.469G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.658G>A
  hgvsp: ENSP00000321698.3:p.Ala220Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.7G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.658G>A
  hgvsp: ENSP00000442792.1:p.Ala220Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.832G>A
  hgvsp: ENSP00000411827.1:p.Ala278Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-251G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.658G>A
  hgvsp: ENSP00000415698.2:p.Ala220Thr
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala278Thr
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: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-64055562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055562
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055562
    reference: chr 11
allele count: 1599
allele frequency: 1.343110573530894e-2
allele num: 119052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.659C>T
  hgvsp: ENSP00000442792.1:p.Ala220Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-250C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.659C>T
  hgvsp: ENSP00000321698.3:p.Ala220Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.659C>T
  hgvsp: ENSP00000415698.2:p.Ala220Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.659C>T
  hgvsp: ENSP00000441003.1:p.Ala220Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+144C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000445570
  ensembl transcript: ENST00000546139
  gene symbol: GPR137
  hgvsc: ENST00000546139.1:c.677C>T
  hgvsp: ENST00000546139.1:c.677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.8C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438716
  ensembl transcript: ENST00000539833
  gene symbol: GPR137
  hgvsc: ENST00000539833.1:c.659C>T
  hgvsp: ENST00000539833.1:c.659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.833C>T
  hgvsp: ENSP00000411827.1:p.Ala278Val
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8319
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 798
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 6.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 10114
  bin: 3.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala278Val
num of homozygotes: 23
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-64055563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055563
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055563
    reference: chr 11
allele count: 4
allele frequency: 3.354579000335458e-5
allele num: 119240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.660G>A
  hgvsp: ENST00000438980.2:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.834G>A
  hgvsp: ENST00000411458.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-249G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.660G>A
  hgvsp: ENST00000539851.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.9G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+145G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.660G>A
  hgvsp: ENST00000543383.1:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.660G>A
  hgvsp: ENST00000313074.3:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21586
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6003
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala278Ala
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

11-64055569-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055569
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055569
    reference: chr 11
allele count: 1
allele frequency: 8.37058242512514e-6
allele num: 119466
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.666T>C
  hgvsp: ENST00000313074.3:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.840T>C
  hgvsp: ENST00000411458.1:c.840T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.15T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+151T>C
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.666T>C
  hgvsp: ENST00000438980.2:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.666T>C
  hgvsp: ENST00000539851.1:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.666T>C
  hgvsp: ENST00000543383.1:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-243T>C
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3914
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly280Gly
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

11-64055572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055572
    reference: chr 11
allele count: 8
allele frequency: 6.68985817500669e-5
allele num: 119584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.669C>T
  hgvsp: ENST00000543383.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-240C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+154C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.843C>T
  hgvsp: ENST00000411458.1:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.669C>T
  hgvsp: ENST00000313074.3:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.669C>T
  hgvsp: ENST00000438980.2:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.18C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.669C>T
  hgvsp: ENST00000539851.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10170
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly281Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

11-64055573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055573
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055573
    reference: chr 11
allele count: 3
allele frequency: 2.50731299623903e-5
allele num: 119650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.670G>A
  hgvsp: ENSP00000442792.1:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-239G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.19G>A
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.670G>A
  hgvsp: ENSP00000321698.3:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.844G>A
  hgvsp: ENSP00000411827.1:p.Ala282Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.670G>A
  hgvsp: ENSP00000415698.2:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.670G>A
  hgvsp: ENSP00000441003.1:p.Ala224Thr
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+155G>A
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6051
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala282Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-64055576-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055576
    reference: chr 11
allele count: 1
allele frequency: 8.353381448810478e-6
allele num: 119712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000441003
  ensembl transcript: ENST00000543383
  gene symbol: GPR137
  hgvsc: ENST00000543383.1:c.673A>G
  hgvsp: ENSP00000441003.1:p.Met225Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-236A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000366931
  ensembl transcript: ENST00000377702
  gene symbol: GPR137
  hgvsc: ENST00000377702.4:c.633+158A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.673A>G
  hgvsp: ENSP00000321698.3:p.Met225Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.673A>G
  hgvsp: ENSP00000442792.1:p.Met225Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.22A>G
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.847A>G
  hgvsp: ENSP00000411827.1:p.Met283Val
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.673A>G
  hgvsp: ENSP00000415698.2:p.Met225Val
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4352
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3919
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met283Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

11-64055581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 64055581
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 64055581
    reference: chr 11
allele count: 1
allele frequency: 8.345155637152633e-6
allele num: 119830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173264
  ensembl transcript: ENST00000545366
  gene symbol: GPR137
  hgvsc: ENST00000545366.1:n.27C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000415698
  ensembl transcript: ENST00000438980
  gene symbol: GPR137
  hgvsc: ENST00000438980.2:c.678C>T
  hgvsp: ENST00000438980.2:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000411827
  ensembl transcript: ENST00000411458
  gene symbol: GPR137
  hgvsc: ENST00000411458.1:c.852C>T
  hgvsp: ENST00000411458.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000438146
  ensembl transcript: ENST00000546201
  gene symbol: GPR137
  hgvsc: ENST00000546201.1:c.408-231C>T
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000442792
  ensembl transcript: ENST00000539851
  gene symbol: GPR137
  hgvsc: ENST00000539851.1:c.678C>T
  hgvsp: ENST00000539851.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173264
  ensembl protein: ENSP00000321698
  ensembl transcript: ENST00000313074
  gene symbol: GPR137
  hgvsc: ENST00000313074.3:c.678C>T
  hgvsp: ENST00000313074.3:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24300
canonical: true
consequence: synonymous
filter: PASS
hgvs: p.Val284Val
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 767
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2119
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12133
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1279
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 136
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3660
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20607
bin: 9.75e1
variant carriers: 14

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

East Asian
type: Population
allele count: 14
allele frequency: 1.62639405204461e-3
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.04e0

FS
type: SiteQuality
SIO_000300: 2.682e0

DP
type: SiteQuality
SIO_000300: 2.196954e6

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

QD
type: SiteQuality
SIO_000300: 1.014e1

GenotypeDepth
all individuals: 229
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10465
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1279
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2118
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20600
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3277
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

FS
type: SiteQuality
SIO_000300: 4.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ReadPosRankSum
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MQRankSum
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QD
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DP
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

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

South Asian
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allele frequency: 3.029568589432865e-4
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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 count: 1
allele frequency: 1.526251526251526e-5
allele num: 65520
num of homozygotes: 0

Other
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allele num: 888
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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South Asian
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allele num: 16504
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European (Finnish)
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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SIO_000300: 2.19701e6

ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

East Asian
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African
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Latino
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European (Finnish)
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num of homozygotes: 0

South Asian
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Other
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DP
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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South Asian
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European (Finnish)
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 1

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

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

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

African
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allele count: 1
allele frequency: 9.813542688910697e-5
allele num: 10190
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.586735161911751e-5
allele num: 65406
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

Latino
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allele count: 6
allele frequency: 5.212858384013901e-4
allele num: 11510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.564e0

ClippingRankSum
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VQSLOD
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DP
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QD
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InbreedingCoeff
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SIO_000300: -9.0e-4

MQRankSum
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BaseQRankSum
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SIO_000300: 5.16e-1

MQ
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SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52895847348786e-5
allele num: 65404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.926e0

MQ
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SIO_000300: 5.953e1

InbreedingCoeff
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SIO_000300: -7.0e-4

ReadPosRankSum
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SIO_000300: 5.93e-1

MQRankSum
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DP
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QD
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ClippingRankSum
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SIO_000300: -4.12e-1

VQSLOD
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BaseQRankSum
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SIO_000300: 5.0e-2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530784067599424e-5
allele num: 65326
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 3.26e-1

MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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SIO_000300: -9.330000000000001e-1

FS
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SIO_000300: 1.379e0

BaseQRankSum
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QD
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DP
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SIO_000300: 2.185627e6

VQSLOD
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SIO_000300: 1.58e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.83477576711251e-5
allele num: 10168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65328
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.859e0

ClippingRankSum
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SIO_000300: -8.57e-1

DP
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MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: 2.2e-3

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.445e-1

QD
type: SiteQuality
SIO_000300: 1.053e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.228840895825013e-4
allele num: 65102
num of homozygotes: 0

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

East Asian
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allele count: 0
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DP
type: SiteQuality
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 2.002803925495694e-4
allele num: 9986
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64936
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11502
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South Asian
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Other
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DP
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ReadPosRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.091476798466627e-5
allele num: 64694
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 1.978584729981378e-3
allele num: 8592
num of homozygotes: 0

African
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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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South Asian
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Other
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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African
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Other
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ReadPosRankSum
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QD
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DP
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

Other
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East Asian
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South Asian
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African
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Latino
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European (Finnish)
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num of homozygotes: 0

FS
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QD
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 5.2e-3

BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 64708
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European (Finnish)
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Latino
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East Asian
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allele num: 8588
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African
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BaseQRankSum
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SIO_000300: 3.49e-1

ClippingRankSum
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SIO_000300: 1.49e-1

MQRankSum
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FS
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MQ
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 5.2e-3

DP
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SIO_000300: 2.156933e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 64370
num of homozygotes: 0

European (Finnish)
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allele frequency: 7.732755954222085e-4
allele num: 6466
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Other
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East Asian
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Non-Finnish)
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allele num: 64342
num of homozygotes: 0

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

European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Other
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African
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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African
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Latino
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European (Finnish)
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Other
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QD
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

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

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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MQRankSum
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QD
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DP
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MQ
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 9678
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.553132668592551e-5
allele num: 64386
num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: 5.43e-1

ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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DP
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MQ
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QD
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BaseQRankSum
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SIO_000300: -4.094e0

VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6506
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South Asian
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allele num: 16496
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.030502885408079e-4
allele num: 9704
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -2.59e-1

DP
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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FS
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SIO_000300: 2.345e0

BaseQRankSum
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SIO_000300: -2.671e0

VQSLOD
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SIO_000300: 1.01e0

ClippingRankSum
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SIO_000300: 9.8e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
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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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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 64354
num of homozygotes: 0

South Asian
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 7.34e-1

QD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.108292925525301e-5
allele num: 64344
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.169999999999999e-1

VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 8.120000000000001e-1

GenotypeDepth
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variant carriers: 1

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

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

African
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allele frequency: 2.321164802700992e-3
allele num: 9478
num of homozygotes: 0

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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South Asian
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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DP
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 3
allele frequency: 2.608242044861763e-4
allele num: 11502
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.248868213181804e-4
allele num: 64058
num of homozygotes: 0

African
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East Asian
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South Asian
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European (Finnish)
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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East Asian
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VQSLOD
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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QD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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Other
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Latino
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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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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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Other
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East Asian
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Latino
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European (Non-Finnish)
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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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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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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African
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Latino
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558846453624318e-5
allele num: 64150
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.312e1

VQSLOD
type: SiteQuality
SIO_000300: -4.713e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

DP
type: SiteQuality
SIO_000300: 2.173251e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.806e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 6.643e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 32

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64160
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

South Asian
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allele count: 32
allele frequency: 1.940099430095792e-3
allele num: 16494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 2.175832e6

BaseQRankSum
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SIO_000300: -3.635e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

QD
type: SiteQuality
SIO_000300: 1.1e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.115070712105165e-5
allele num: 64204
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.174839e6

FS
type: SiteQuality
SIO_000300: 4.788e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.426e1

GenotypeQuality
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bin: 5.75e1
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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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557438325442313e-5
allele num: 64208
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

DP
type: SiteQuality
SIO_000300: 2.176092e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 9.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.062473438164046e-4
allele num: 9412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

DP
type: SiteQuality
SIO_000300: 2.176092e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.903e0

FS
type: SiteQuality
SIO_000300: 9.11e-1

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.054852320675106e-4
allele num: 9480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64306
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.869e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64314
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

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

South Asian
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allele count: 5
allele frequency: 3.03030303030303e-4
allele num: 16500
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.553615262716341e-5
allele num: 64366
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11522
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African
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South Asian
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VQSLOD
type: SiteQuality
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

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

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.088230752601834e-5
allele num: 64762
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

DP
type: SiteQuality
SIO_000300: 2.18984e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

FS
type: SiteQuality
SIO_000300: 1.727e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

GenotypeDepth
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 60

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

GenotypeQuality
all individuals: 13309
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.707723138584863e-5
allele num: 64870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

Other
type: Population
allele count: 4
allele frequency: 4.524886877828055e-3
allele num: 884
num of homozygotes: 1

African
type: Population
allele count: 2
allele frequency: 2.016942315449778e-4
allele num: 9916
num of homozygotes: 0

Latino
type: Population
allele count: 51
allele frequency: 4.423243712055508e-3
allele num: 11530
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
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SIO_000300: 1.338e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

DP
type: SiteQuality
SIO_000300: 2.195394e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
all individuals: 4427
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GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.158962830659316e-5
allele num: 64946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.328e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

DP
type: SiteQuality
SIO_000300: 2.19669e6

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1572

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1270
allele frequency: 1.954447522314558e-2
allele num: 64980
num of homozygotes: 17

African
type: Population
allele count: 31
allele frequency: 3.111824934752058e-3
allele num: 9962
num of homozygotes: 1

Other
type: Population
allele count: 13
allele frequency: 1.470588235294118e-2
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 62
allele frequency: 5.377276669557675e-3
allele num: 11530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 124
allele frequency: 1.875945537065053e-2
allele num: 6610
num of homozygotes: 2

East Asian
type: Population
allele count: 34
allele frequency: 3.961780470752739e-3
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 65
allele frequency: 3.938439166262724e-3
allele num: 16504
num of homozygotes: 3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 2.288127e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 6.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 61
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3438
bin: 7.25e1
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GenotypeQuality
all individuals: 2561
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.072196620583717e-5
allele num: 65100
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.03e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.139e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.263303e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 21589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 68
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65258
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.425e0

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

DP
type: SiteQuality
SIO_000300: 2.266616e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-1

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
all individuals: 3366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 52
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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: 172
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4335
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GenotypeQuality
all individuals: 21597
bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 4
allele frequency: 3.955696202531646e-4
allele num: 10112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.121449559255632e-5
allele num: 65344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.723e0

VQSLOD
type: SiteQuality
SIO_000300: 5.8e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

DP
type: SiteQuality
SIO_000300: 2.267925e6

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.26877e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

FS
type: SiteQuality
SIO_000300: 4.069e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.42e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.32e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13721
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GenotypeQuality
all individuals: 867
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GenotypeQuality
all individuals: 3457
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GenotypeQuality
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GenotypeQuality
all individuals: 2564
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GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528023959415684e-5
allele num: 65444
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.269806e6

QD
type: SiteQuality
SIO_000300: 1.378e1