22-24829329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829329
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829329
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 12342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1092G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-927C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-44G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5635G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-927C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28668
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23861
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

22-24829338-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829338
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829338
    reference: chr 22
allele count: 998
allele frequency: 5.207137639570072e-2
allele num: 19166
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1101C>G
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-936G>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5644C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-936G>C
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 2.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 1.25e1
  variant carriers: 350
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32810
  bin: 7.5e0
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 2.25e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 2.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 54
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS

22-24829338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829338
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829338
    reference: chr 22
allele count: 3
allele frequency: 1.565271835542106e-4
allele num: 19166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-936G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1101C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-936G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5644C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-35C>T
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32810
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

22-24829340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829340
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829340
    reference: chr 22
allele count: 2
allele frequency: 9.302325581395348e-5
allele num: 21500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-938G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1103C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-938G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5646C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-33C>T
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

22-24829341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829341
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829341
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 23688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5647G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-939C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1104G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-32G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-939C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35381
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

22-24829344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829344
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829344
    reference: chr 22
allele count: 1
allele frequency: 3.767045882618851e-5
allele num: 26546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-942G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5650C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-942G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-29C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1107C>T
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4104
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36369
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

22-24829345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829345
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829345
    reference: chr 22
allele count: 3
allele frequency: 1.05708245243129e-4
allele num: 28380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-943C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1108G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-28G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5651G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-943C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36616
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

22-24829362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829362
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829362
    reference: chr 22
allele count: 3
allele frequency: 6.236487610177948e-5
allele num: 48104
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-960G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5668C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1125C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-960G>A
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33163
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

22-24829363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829363
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829363
    reference: chr 22
allele count: 7
allele frequency: 1.378224059854302e-4
allele num: 50790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1126G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-961C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5669G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-961C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32281
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

22-24829367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829367
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829367
    reference: chr 22
allele count: 1
allele frequency: 1.768471686768295e-5
allele num: 56546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1130G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5673G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-965C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-965C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-6G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

22-24829575-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829575
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829575
    reference: chr 22
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.203C>T
  hgvsp: ENSP00000473799.1:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.203C>T
  hgvsp: ENSP00000400190.1:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1173G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.203C>T
  hgvsp: ENSP00000474097.1:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.203C>T
  hgvsp: ENSP00000414802.2:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.203C>T
  hgvsp: ENSP00000404497.1:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1173G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.203C>T
  hgvsp: ENSP00000336630.6:p.Thr68Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1338C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5881C>T
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55041
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr68Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

22-24829371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829371
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829371
    reference: chr 22
allele count: 1
allele frequency: 1.633133002351711e-5
allele num: 61232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-969G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1134C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-969G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5677C>T
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4964
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

22-24829383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829383
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829383
    reference: chr 22
allele count: 10
allele frequency: 1.264286436735107e-4
allele num: 79096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.11T>C
  hgvsp: ENSP00000475000.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.11T>C
  hgvsp: ENSP00000336630.6:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.11T>C
  hgvsp: ENSP00000400190.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.11T>C
  hgvsp: ENSP00000404497.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.11T>C
  hgvsp: ENSP00000474895.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5689T>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.11T>C
  hgvsp: ENSP00000473799.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.11T>C
  hgvsp: ENSP00000397071.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-981A>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.11T>C
  hgvsp: ENSP00000474097.1:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.11T>C
  hgvsp: ENSP00000414802.2:p.Met4Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-981A>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1146T>C
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28158
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20359
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met4Thr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

22-24829389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829389
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829389
    reference: chr 22
allele count: 1
allele frequency: 1.138355758941785e-5
allele num: 87846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.17C>T
  hgvsp: ENSP00000397071.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.17C>T
  hgvsp: ENSP00000414802.2:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-987G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-987G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.17C>T
  hgvsp: ENSP00000336630.6:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1152C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.17C>T
  hgvsp: ENSP00000475000.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.17C>T
  hgvsp: ENSP00000474895.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.17C>T
  hgvsp: ENSP00000400190.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.17C>T
  hgvsp: ENSP00000474097.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.17C>T
  hgvsp: ENSP00000404497.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5695C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.17C>T
  hgvsp: ENSP00000473799.1:p.Ser6Phe
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31986
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser6Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

22-24829390-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829390
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829390
    reference: chr 22
allele count: 1
allele frequency: 1.116495098586517e-5
allele num: 89566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.18C>T
  hgvsp: ENST00000444262.2:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.18C>T
  hgvsp: ENST00000337539.7:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.18C>T
  hgvsp: ENST00000496258.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.18C>T
  hgvsp: ENST00000439591.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-988G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-988G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1153C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.18C>T
  hgvsp: ENST00000424232.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.18C>T
  hgvsp: ENST00000436735.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5696C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.18C>T
  hgvsp: ENST00000486108.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474895
  ensembl transcript: ENST00000464977
  gene symbol: ADORA2A
  hgvsc: ENST00000464977.1:c.18C>T
  hgvsp: ENST00000464977.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.18C>T
  hgvsp: ENST00000472248.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5653
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser6Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

22-24829392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829392
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829392
    reference: chr 22
allele count: 1
allele frequency: 1.084292932578665e-5
allele num: 92226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.20C>T
  hgvsp: ENSP00000474097.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.20C>T
  hgvsp: ENSP00000400190.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1155C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.20C>T
  hgvsp: ENSP00000336630.6:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.20C>T
  hgvsp: ENSP00000475000.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-990G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.20C>T
  hgvsp: ENSP00000473799.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.20C>T
  hgvsp: ENSP00000414802.2:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.20C>T
  hgvsp: ENSP00000397071.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5698C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.20C>T
  hgvsp: ENSP00000404497.1:p.Ser7Leu
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-990G>A
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14037
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser7Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

22-24829393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829393
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829393
    reference: chr 22
allele count: 9
allele frequency: 9.364270107168869e-5
allele num: 96110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.21G>A
  hgvsp: ENST00000424232.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.21G>A
  hgvsp: ENST00000436735.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.21G>A
  hgvsp: ENST00000486108.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1156G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-991C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.21G>A
  hgvsp: ENST00000496258.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.21G>A
  hgvsp: ENST00000337539.7:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-991C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.21G>A
  hgvsp: ENST00000444262.2:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.21G>A
  hgvsp: ENST00000472248.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.21G>A
  hgvsp: ENST00000439591.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5699G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36264
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser7Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

22-24829393-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829393
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829393
    reference: chr 22
allele count: 6
allele frequency: 6.242846738112579e-5
allele num: 96110
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-991C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.21G>C
  hgvsp: ENST00000439591.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1156G>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-991C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.21G>C
  hgvsp: ENST00000472248.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.21G>C
  hgvsp: ENST00000496258.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.21G>C
  hgvsp: ENST00000337539.7:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.21G>C
  hgvsp: ENST00000444262.2:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.21G>C
  hgvsp: ENST00000436735.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5699G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.21G>C
  hgvsp: ENST00000486108.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.21G>C
  hgvsp: ENST00000424232.1:c.21G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36264
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser7Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

22-24829395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829395
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829395
    reference: chr 22
allele count: 2
allele frequency: 1.997922160952609e-5
allele num: 100104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-993A>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.23T>C
  hgvsp: ENSP00000474097.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.23T>C
  hgvsp: ENSP00000336630.6:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.23T>C
  hgvsp: ENSP00000473799.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.23T>C
  hgvsp: ENSP00000414802.2:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5701T>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.23T>C
  hgvsp: ENSP00000404497.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.23T>C
  hgvsp: ENSP00000400190.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.23T>C
  hgvsp: ENSP00000475000.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.23T>C
  hgvsp: ENSP00000397071.1:p.Val8Ala
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1158T>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-993A>G
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38268
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val8Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

22-24829396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829396
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829396
    reference: chr 22
allele count: 1
allele frequency: 9.902754946426096e-6
allele num: 100982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.24G>A
  hgvsp: ENST00000472248.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.24G>A
  hgvsp: ENST00000424232.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.24G>A
  hgvsp: ENST00000436735.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.24G>A
  hgvsp: ENST00000337539.7:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.24G>A
  hgvsp: ENST00000486108.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.24G>A
  hgvsp: ENST00000496258.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1159G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5702G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-994C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-994C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.24G>A
  hgvsp: ENST00000439591.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.24G>A
  hgvsp: ENST00000444262.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38440
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val8Val
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

22-24829396-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829396
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829396
    reference: chr 22
allele count: 1
allele frequency: 9.902754946426096e-6
allele num: 100982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.24G>C
  hgvsp: ENST00000439591.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.24G>C
  hgvsp: ENST00000472248.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.24G>C
  hgvsp: ENST00000337539.7:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.24G>C
  hgvsp: ENST00000424232.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5702G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.24G>C
  hgvsp: ENST00000496258.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.24G>C
  hgvsp: ENST00000444262.2:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.24G>C
  hgvsp: ENST00000436735.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.24G>C
  hgvsp: ENST00000486108.1:c.24G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-994C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1159G>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-994C>G
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val8Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

22-24829404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829404
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829404
    reference: chr 22
allele count: 1
allele frequency: 9.194725905220765e-6
allele num: 108758
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1002G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1167C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.32C>T
  hgvsp: ENSP00000400190.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.32C>T
  hgvsp: ENSP00000475000.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.32C>T
  hgvsp: ENSP00000414802.2:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.32C>T
  hgvsp: ENSP00000336630.6:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.32C>T
  hgvsp: ENSP00000404497.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5710C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.32C>T
  hgvsp: ENSP00000397071.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.32C>T
  hgvsp: ENSP00000473799.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.32C>T
  hgvsp: ENSP00000474097.1:p.Thr11Met
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1002G>A
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41813
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr11Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

22-24829405-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829405
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829405
    reference: chr 22
allele count: 6
allele frequency: 5.463386206770957e-5
allele num: 109822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.33G>A
  hgvsp: ENST00000486108.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5711G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.33G>A
  hgvsp: ENST00000496258.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1003C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.33G>A
  hgvsp: ENST00000444262.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1168G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.33G>A
  hgvsp: ENST00000424232.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1003C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.33G>A
  hgvsp: ENST00000337539.7:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.33G>A
  hgvsp: ENST00000439591.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.33G>A
  hgvsp: ENST00000436735.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.33G>A
  hgvsp: ENST00000472248.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr11Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

22-24829411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829411
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829411
    reference: chr 22
allele count: 1
allele frequency: 8.810417437578192e-6
allele num: 113502
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.39G>A
  hgvsp: ENST00000337539.7:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.39G>A
  hgvsp: ENST00000439591.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.39G>A
  hgvsp: ENST00000496258.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.39G>A
  hgvsp: ENST00000424232.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1009C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1009C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.39G>A
  hgvsp: ENST00000472248.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.39G>A
  hgvsp: ENST00000444262.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5717G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.39G>A
  hgvsp: ENST00000486108.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.39G>A
  hgvsp: ENST00000436735.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1174G>A
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu13Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

22-24829414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829414
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829414
    reference: chr 22
allele count: 2
allele frequency: 1.737287399454492e-5
allele num: 115122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.42G>A
  hgvsp: ENST00000472248.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.42G>A
  hgvsp: ENST00000439591.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1012C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.42G>A
  hgvsp: ENST00000424232.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5720G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.42G>A
  hgvsp: ENST00000444262.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.42G>A
  hgvsp: ENST00000496258.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1177G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.42G>A
  hgvsp: ENST00000436735.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.42G>A
  hgvsp: ENST00000337539.7:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1012C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.42G>A
  hgvsp: ENST00000486108.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu14Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

22-24829415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829415
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829415
    reference: chr 22
allele count: 10
allele frequency: 8.652614820198664e-5
allele num: 115572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.43G>A
  hgvsp: ENSP00000473799.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1178G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.43G>A
  hgvsp: ENSP00000475000.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5721G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.43G>A
  hgvsp: ENSP00000474097.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.43G>A
  hgvsp: ENSP00000404497.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.43G>A
  hgvsp: ENSP00000400190.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.43G>A
  hgvsp: ENSP00000336630.6:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.43G>A
  hgvsp: ENSP00000414802.2:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.43G>A
  hgvsp: ENSP00000397071.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1013C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1013C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43666
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala15Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

22-24829429-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829429
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829429
    reference: chr 22
allele count: 2
allele frequency: 1.677599020282172e-5
allele num: 119218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.57G>A
  hgvsp: ENST00000444262.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1027C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.57G>A
  hgvsp: ENST00000496258.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.57G>A
  hgvsp: ENST00000424232.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5735G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.57G>A
  hgvsp: ENST00000472248.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.57G>A
  hgvsp: ENST00000337539.7:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.57G>A
  hgvsp: ENST00000436735.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.57G>A
  hgvsp: ENST00000486108.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1027C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.57G>A
  hgvsp: ENST00000439591.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1192G>A
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu19Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

22-24829433-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829433
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829433
    reference: chr 22
allele count: 4
allele frequency: 3.339957582538702e-5
allele num: 119762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.61A>G
  hgvsp: ENSP00000404497.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.61A>G
  hgvsp: ENSP00000397071.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.61A>G
  hgvsp: ENSP00000473799.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5739A>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.61A>G
  hgvsp: ENSP00000400190.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1031T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.61A>G
  hgvsp: ENSP00000474097.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.61A>G
  hgvsp: ENSP00000336630.6:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.61A>G
  hgvsp: ENSP00000475000.1:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1031T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.61A>G
  hgvsp: ENSP00000414802.2:p.Ile21Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1196A>G
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile21Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

22-24829440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829440
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829440
    reference: chr 22
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1038C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1203G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.68G>A
  hgvsp: ENSP00000336630.6:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.68G>A
  hgvsp: ENSP00000473799.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5746G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.68G>A
  hgvsp: ENSP00000404497.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.68G>A
  hgvsp: ENSP00000397071.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.68G>A
  hgvsp: ENSP00000475000.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1038C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.68G>A
  hgvsp: ENSP00000414802.2:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.68G>A
  hgvsp: ENSP00000474097.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.68G>A
  hgvsp: ENSP00000400190.1:p.Gly23Asp
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly23Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

22-24829443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829443
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829443
    reference: chr 22
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.71A>G
  hgvsp: ENSP00000474097.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.71A>G
  hgvsp: ENSP00000336630.6:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5749A>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.71A>G
  hgvsp: ENSP00000404497.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1041T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.71A>G
  hgvsp: ENSP00000414802.2:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1041T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.71A>G
  hgvsp: ENSP00000397071.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.71A>G
  hgvsp: ENSP00000400190.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.71A>G
  hgvsp: ENSP00000475000.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.71A>G
  hgvsp: ENSP00000473799.1:p.Asn24Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1206A>G
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn24Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

22-24829451-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829451
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829452
    reference: chr 22
allele count: 2
allele frequency: 1.655492095025246e-5
allele num: 120810
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5758dupT
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.80dupT
  hgvsp: ENSP00000414802.2:p.Cys28ValfsTer74
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.80dupT
  hgvsp: ENSP00000397071.1:p.Cys28ValfsTer?
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1215dupT
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1050dupA
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.80dupT
  hgvsp: ENSP00000336630.6:p.Cys28ValfsTer74
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1050dupA
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.80dupT
  hgvsp: ENSP00000404497.1:p.Cys28ValfsTer?
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.80dupT
  hgvsp: ENSP00000473799.1:p.Cys28ValfsTer74
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.80dupT
  hgvsp: ENSP00000474097.1:p.Cys28ValfsTer?
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.80dupT
  hgvsp: ENSP00000475000.1:p.Cys28ValfsTer?
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.80dupT
  hgvsp: ENSP00000400190.1:p.Cys28ValfsTer?
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys28ValfsTer74
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-24829453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829453
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829453
    reference: chr 22
allele count: 3
allele frequency: 2.481964392084188e-5
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.81G>A
  hgvsp: ENST00000337539.7:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1051C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1216G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.81G>A
  hgvsp: ENST00000496258.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5759G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.81G>A
  hgvsp: ENST00000424232.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.81G>A
  hgvsp: ENST00000472248.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.81G>A
  hgvsp: ENST00000444262.2:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.81G>A
  hgvsp: ENST00000486108.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1051C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.81G>A
  hgvsp: ENST00000436735.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.81G>A
  hgvsp: ENST00000439591.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val27Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-24829455-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829455
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829455
    reference: chr 22
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.83G>C
  hgvsp: ENSP00000473799.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.83G>C
  hgvsp: ENSP00000397071.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5761G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.83G>C
  hgvsp: ENSP00000336630.6:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.83G>C
  hgvsp: ENSP00000474097.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1218G>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1053C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.83G>C
  hgvsp: ENSP00000404497.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000475000
  ensembl transcript: ENST00000472248
  gene symbol: ADORA2A
  hgvsc: ENST00000472248.1:c.83G>C
  hgvsp: ENSP00000475000.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1053C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.83G>C
  hgvsp: ENSP00000400190.1:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.83G>C
  hgvsp: ENSP00000414802.2:p.Cys28Ser
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys28Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

22-24829470-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829470
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829470
    reference: chr 22
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.98T>G
  hgvsp: ENSP00000397071.1:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.98T>G
  hgvsp: ENSP00000336630.6:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5776T>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1233T>G
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.98T>G
  hgvsp: ENSP00000414802.2:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.98T>G
  hgvsp: ENSP00000473799.1:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.98T>G
  hgvsp: ENSP00000404497.1:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1068A>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1068A>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.98T>G
  hgvsp: ENSP00000400190.1:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.98T>G
  hgvsp: ENSP00000474097.1:p.Leu33Arg
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu33Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-24829474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829474
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829474
    reference: chr 22
allele count: 3
allele frequency: 2.47610558114198e-5
allele num: 121158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.102C>T
  hgvsp: ENST00000444262.2:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.102C>T
  hgvsp: ENST00000496258.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1237C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1072G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1072G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5780C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.102C>T
  hgvsp: ENST00000424232.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.102C>T
  hgvsp: ENST00000337539.7:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.102C>T
  hgvsp: ENST00000436735.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.102C>T
  hgvsp: ENST00000439591.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.102C>T
  hgvsp: ENST00000486108.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn34Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

22-24829489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829489
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829489
    reference: chr 22
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.117C>T
  hgvsp: ENST00000436735.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.117C>T
  hgvsp: ENST00000444262.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5795C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.117C>T
  hgvsp: ENST00000424232.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.117C>T
  hgvsp: ENST00000337539.7:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1252C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.117C>T
  hgvsp: ENST00000496258.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.117C>T
  hgvsp: ENST00000439591.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1087G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.117C>T
  hgvsp: ENST00000486108.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1087G>A
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn39Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-24829490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829490
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829490
    reference: chr 22
allele count: 23
allele frequency: 1.897188861026791e-4
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.118G>A
  hgvsp: ENSP00000336630.6:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.118G>A
  hgvsp: ENSP00000473799.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.118G>A
  hgvsp: ENSP00000397071.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.118G>A
  hgvsp: ENSP00000400190.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.118G>A
  hgvsp: ENSP00000404497.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.118G>A
  hgvsp: ENSP00000474097.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5796G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1253G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.118G>A
  hgvsp: ENSP00000414802.2:p.Val40Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1088C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1088C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val40Ile
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

22-24829491-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829491
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829491
    reference: chr 22
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1254T>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1089A>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.119T>A
  hgvsp: ENSP00000400190.1:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.119T>A
  hgvsp: ENSP00000474097.1:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.119T>A
  hgvsp: ENSP00000397071.1:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.119T>A
  hgvsp: ENSP00000414802.2:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.119T>A
  hgvsp: ENSP00000404497.1:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.119T>A
  hgvsp: ENSP00000336630.6:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1089A>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.119T>A
  hgvsp: ENSP00000473799.1:p.Val40Asp
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5797T>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val40Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

22-24829507-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829507
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829507
    reference: chr 22
allele count: 3
allele frequency: 2.473941153186436e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.135G>C
  hgvsp: ENST00000424232.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1105C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.135G>C
  hgvsp: ENST00000486108.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1270G>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5813G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.135G>C
  hgvsp: ENST00000436735.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.135G>C
  hgvsp: ENST00000439591.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.135G>C
  hgvsp: ENST00000337539.7:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.135G>C
  hgvsp: ENST00000496258.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1105C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.135G>C
  hgvsp: ENST00000444262.2:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val45Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-24829516-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829516
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829516
    reference: chr 22
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.144G>C
  hgvsp: ENST00000424232.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.144G>C
  hgvsp: ENST00000337539.7:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.144G>C
  hgvsp: ENST00000436735.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1114C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5822G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.144G>C
  hgvsp: ENST00000439591.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.144G>C
  hgvsp: ENST00000496258.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1114C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.144G>C
  hgvsp: ENST00000486108.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.144G>C
  hgvsp: ENST00000444262.2:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1279G>C
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu48Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

22-24829518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829518
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829518
    reference: chr 22
allele count: 5
allele frequency: 4.128750970256478e-5
allele num: 121102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1116G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.146C>T
  hgvsp: ENSP00000404497.1:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.146C>T
  hgvsp: ENSP00000473799.1:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.146C>T
  hgvsp: ENSP00000474097.1:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1116G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1281C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5824C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.146C>T
  hgvsp: ENSP00000336630.6:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.146C>T
  hgvsp: ENSP00000400190.1:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.146C>T
  hgvsp: ENSP00000414802.2:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.146C>T
  hgvsp: ENSP00000397071.1:p.Ala49Val
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala49Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

22-24829519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829519
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829519
    reference: chr 22
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.147G>A
  hgvsp: ENST00000337539.7:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.147G>A
  hgvsp: ENST00000424232.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.147G>A
  hgvsp: ENST00000486108.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.147G>A
  hgvsp: ENST00000444262.2:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1282G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1117C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.147G>A
  hgvsp: ENST00000439591.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.147G>A
  hgvsp: ENST00000436735.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.147G>A
  hgvsp: ENST00000496258.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1117C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5825G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala49Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

22-24829521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829521
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829521
    reference: chr 22
allele count: 306
allele frequency: 2.530473181945984e-3
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1119G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.149C>T
  hgvsp: ENSP00000397071.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5827C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1284C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.149C>T
  hgvsp: ENSP00000473799.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.149C>T
  hgvsp: ENSP00000336630.6:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1119G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.149C>T
  hgvsp: ENSP00000404497.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.149C>T
  hgvsp: ENSP00000400190.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.149C>T
  hgvsp: ENSP00000414802.2:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.149C>T
  hgvsp: ENSP00000474097.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 44031
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13336
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Ala50Val
num of homozygotes: 7
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

22-24829522-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829522
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829522
    reference: chr 22
allele count: 12
allele frequency: 9.904912836767037e-5
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.150G>A
  hgvsp: ENST00000496258.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.150G>A
  hgvsp: ENST00000444262.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1120C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.150G>A
  hgvsp: ENST00000486108.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5828G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.150G>A
  hgvsp: ENST00000424232.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.150G>A
  hgvsp: ENST00000439591.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.150G>A
  hgvsp: ENST00000436735.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.150G>A
  hgvsp: ENST00000337539.7:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1120C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1285G>A
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala50Ala
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

22-24829525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829525
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829525
    reference: chr 22
allele count: 5
allele frequency: 4.127183279955096e-5
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.153C>T
  hgvsp: ENST00000486108.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.153C>T
  hgvsp: ENST00000436735.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.153C>T
  hgvsp: ENST00000337539.7:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1123G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1123G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1288C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5831C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.153C>T
  hgvsp: ENST00000496258.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.153C>T
  hgvsp: ENST00000424232.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.153C>T
  hgvsp: ENST00000439591.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.153C>T
  hgvsp: ENST00000444262.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala51Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

22-24829526-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829526
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829526
    reference: chr 22
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.154G>A
  hgvsp: ENSP00000397071.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1124C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.154G>A
  hgvsp: ENSP00000336630.6:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.154G>A
  hgvsp: ENSP00000473799.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.154G>A
  hgvsp: ENSP00000414802.2:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1289G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.154G>A
  hgvsp: ENSP00000400190.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.154G>A
  hgvsp: ENSP00000474097.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.154G>A
  hgvsp: ENSP00000404497.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1124C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5832G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp52Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

22-24829531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829531
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829531
    reference: chr 22
allele count: 3
allele frequency: 2.475942095967516e-5
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.159C>T
  hgvsp: ENST00000496258.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.159C>T
  hgvsp: ENST00000486108.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1294C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.159C>T
  hgvsp: ENST00000337539.7:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5837C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1129G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.159C>T
  hgvsp: ENST00000439591.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.159C>T
  hgvsp: ENST00000436735.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1129G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.159C>T
  hgvsp: ENST00000444262.2:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.159C>T
  hgvsp: ENST00000424232.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile53Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

22-24829532-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829532
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829532
    reference: chr 22
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.160G>A
  hgvsp: ENSP00000400190.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.160G>A
  hgvsp: ENSP00000336630.6:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.160G>A
  hgvsp: ENSP00000397071.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5838G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.160G>A
  hgvsp: ENSP00000404497.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.160G>A
  hgvsp: ENSP00000473799.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1295G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.160G>A
  hgvsp: ENSP00000414802.2:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1130C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1130C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.160G>A
  hgvsp: ENSP00000474097.1:p.Ala54Thr
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala54Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-24829547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829547
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829547
    reference: chr 22
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.175G>A
  hgvsp: ENSP00000400190.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.175G>A
  hgvsp: ENSP00000404497.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.175G>A
  hgvsp: ENSP00000473799.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.175G>A
  hgvsp: ENSP00000336630.6:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.175G>A
  hgvsp: ENSP00000474097.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.175G>A
  hgvsp: ENSP00000397071.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5853G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.175G>A
  hgvsp: ENSP00000414802.2:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1145C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1145C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1310G>A
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala59Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

22-24829549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829549
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829549
    reference: chr 22
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.177C>T
  hgvsp: ENST00000444262.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1147G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.177C>T
  hgvsp: ENST00000424232.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.177C>T
  hgvsp: ENST00000439591.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.177C>T
  hgvsp: ENST00000337539.7:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.177C>T
  hgvsp: ENST00000486108.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1147G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1312C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.177C>T
  hgvsp: ENST00000496258.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.177C>T
  hgvsp: ENST00000436735.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5855C>T
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala59Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

22-24829550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829550
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829550
    reference: chr 22
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1313A>G
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.178A>G
  hgvsp: ENSP00000336630.6:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1148T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.178A>G
  hgvsp: ENSP00000404497.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.178A>G
  hgvsp: ENSP00000473799.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.178A>G
  hgvsp: ENSP00000400190.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.178A>G
  hgvsp: ENSP00000414802.2:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5856A>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000397071
  ensembl transcript: ENST00000436735
  gene symbol: ADORA2A
  hgvsc: ENST00000436735.1:c.178A>G
  hgvsp: ENSP00000397071.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1148T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.178A>G
  hgvsp: ENSP00000474097.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile60Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

22-24829568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829568
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829568
    reference: chr 22
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.196A>G
  hgvsp: ENSP00000474097.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.196A>G
  hgvsp: ENSP00000473799.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1166T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.196A>G
  hgvsp: ENSP00000404497.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.196A>G
  hgvsp: ENSP00000400190.1:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1166T>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.196A>G
  hgvsp: ENSP00000336630.6:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.196A>G
  hgvsp: ENSP00000414802.2:p.Ile66Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1331A>G
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5874A>G
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3768
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile66Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff

22-24829573-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829573
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829573
    reference: chr 22
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.201C>G
  hgvsp: ENSP00000473799.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.201C>G
  hgvsp: ENSP00000400190.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.201C>G
  hgvsp: ENSP00000414802.2:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.201C>G
  hgvsp: ENSP00000336630.6:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1171G>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1336C>G
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.201C>G
  hgvsp: ENSP00000404497.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.201C>G
  hgvsp: ENSP00000474097.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1171G>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5879C>G
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser67Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

22-24829573-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829573
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829573
    reference: chr 22
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.201C>T
  hgvsp: ENST00000439591.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1171G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.201C>T
  hgvsp: ENST00000337539.7:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.201C>T
  hgvsp: ENST00000486108.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.201C>T
  hgvsp: ENST00000444262.2:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.201C>T
  hgvsp: ENST00000496258.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5879C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1336C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1171G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.201C>T
  hgvsp: ENST00000424232.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser67Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

22-24829576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829576
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829576
    reference: chr 22
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.204C>T
  hgvsp: ENST00000486108.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5882C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.204C>T
  hgvsp: ENST00000444262.2:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.204C>T
  hgvsp: ENST00000424232.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1174G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1339C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.204C>T
  hgvsp: ENST00000496258.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.204C>T
  hgvsp: ENST00000337539.7:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1174G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.204C>T
  hgvsp: ENST00000439591.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr68Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

22-24829577-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829577
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829577
    reference: chr 22
allele count: 2
allele frequency: 1.649158104787506e-5
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.205G>A
  hgvsp: ENSP00000404497.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1175C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.205G>A
  hgvsp: ENSP00000336630.6:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1340G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.205G>A
  hgvsp: ENSP00000473799.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.205G>A
  hgvsp: ENSP00000400190.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.205G>A
  hgvsp: ENSP00000474097.1:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5883G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.205G>A
  hgvsp: ENSP00000414802.2:p.Gly69Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1175C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly69Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

22-24829579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829579
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829579
    reference: chr 22
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1177C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.207G>A
  hgvsp: ENST00000486108.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1342G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.207G>A
  hgvsp: ENST00000444262.2:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.207G>A
  hgvsp: ENST00000337539.7:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.207G>A
  hgvsp: ENST00000424232.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1177C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.207G>A
  hgvsp: ENST00000496258.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.207G>A
  hgvsp: ENST00000439591.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5885G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 44179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55048
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly69Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

22-24829586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829586
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829586
    reference: chr 22
allele count: 3
allele frequency: 2.473818751546137e-5
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.214G>A
  hgvsp: ENSP00000400190.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.214G>A
  hgvsp: ENSP00000474097.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1349G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.214G>A
  hgvsp: ENSP00000404497.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5892G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.214G>A
  hgvsp: ENSP00000473799.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1184C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1184C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.214G>A
  hgvsp: ENSP00000414802.2:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.214G>A
  hgvsp: ENSP00000336630.6:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala72Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

22-24829587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829587
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829587
    reference: chr 22
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.215C>T
  hgvsp: ENSP00000336630.6:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.215C>T
  hgvsp: ENSP00000414802.2:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.215C>T
  hgvsp: ENSP00000473799.1:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.215C>T
  hgvsp: ENSP00000474097.1:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1350C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.215C>T
  hgvsp: ENSP00000400190.1:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.215C>T
  hgvsp: ENSP00000404497.1:p.Ala72Val
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1185G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5893C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1185G>A
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala72Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

22-24829597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829597
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829597
    reference: chr 22
allele count: 17
allele frequency: 1.401322188700397e-4
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.225C>T
  hgvsp: ENST00000496258.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.225C>T
  hgvsp: ENST00000444262.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1360C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5903C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000400190
  ensembl transcript: ENST00000439591
  gene symbol: ADORA2A
  hgvsc: ENST00000439591.1:c.225C>T
  hgvsp: ENST00000439591.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1195G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.225C>T
  hgvsp: ENST00000486108.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.225C>T
  hgvsp: ENST00000424232.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1195G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.225C>T
  hgvsp: ENST00000337539.7:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13886
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His75His
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: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-24829615-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829615
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829615
    reference: chr 22
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.243C>T
  hgvsp: ENST00000486108.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.243C>T
  hgvsp: ENST00000496258.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.243C>T
  hgvsp: ENST00000424232.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.243C>T
  hgvsp: ENST00000444262.2:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1213G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5921C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1378C>T
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1213G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.243C>T
  hgvsp: ENST00000337539.7:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala81Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-24829622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829622
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829622
    reference: chr 22
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.250G>A
  hgvsp: ENSP00000473799.1:p.Val84Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1220C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.250G>A
  hgvsp: ENSP00000336630.6:p.Val84Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.250G>A
  hgvsp: ENSP00000414802.2:p.Val84Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1385G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.250G>A
  hgvsp: ENSP00000404497.1:p.Val84Ile
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5928G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1220C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000474097
  ensembl transcript: ENST00000496258
  gene symbol: ADORA2A
  hgvsc: ENST00000496258.1:c.250G>A
  hgvsp: ENST00000496258.1:c.250G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val84Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP

22-24829635-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829635
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829635
    reference: chr 22
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1233G>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.263C>G
  hgvsp: ENSP00000336630.6:p.Thr88Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.263C>G
  hgvsp: ENSP00000414802.2:p.Thr88Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.263C>G
  hgvsp: ENSP00000473799.1:p.Thr88Arg
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000404497
  ensembl transcript: ENST00000424232
  gene symbol: ADORA2A
  hgvsc: ENST00000424232.1:c.263C>G
  hgvsp: ENST00000424232.1:c.263C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5941C>G
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1233G>C
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1398C>G
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3743
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr88Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

22-24829636-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829636
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829636
    reference: chr 22
allele count: 7
allele frequency: 5.769769703763538e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.264G>A
  hgvsp: ENST00000337539.7:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.264G>A
  hgvsp: ENST00000444262.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1399G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1234C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.264G>A
  hgvsp: ENST00000486108.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1234C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5942G>A
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr88Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

22-24829639-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829639
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829639
    reference: chr 22
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.267G>C
  hgvsp: ENSP00000473799.1:p.Gln89His
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1402G>C
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1237C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.267G>C
  hgvsp: ENSP00000336630.6:p.Gln89His
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5945G>C
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1237C>G
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.267G>C
  hgvsp: ENSP00000414802.2:p.Gln89His
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln89His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

22-24829663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829663
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829663
    reference: chr 22
allele count: 11
allele frequency: 9.073511944041178e-5
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1261G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.291C>T
  hgvsp: ENST00000444262.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.291C>T
  hgvsp: ENST00000486108.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5969C>T
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1261G>A
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.291C>T
  hgvsp: ENST00000337539.7:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1426C>T
  variant of: http://identifiers.org/hgnc/49185
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55004
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala97Ala
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

22-24829677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829677
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829677
    reference: chr 22
allele count: 1
allele frequency: 8.262823902696986e-6
allele num: 121024
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1440G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.305G>A
  hgvsp: ENSP00000414802.2:p.Arg102His
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.305G>A
  hgvsp: ENSP00000473799.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.305G>A
  hgvsp: ENSP00000336630.6:p.Arg102His
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1275C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5983G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1275C>T
  variant of: http://identifiers.org/hgnc/37122
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3670
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg102His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

22-24829685-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24829685
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 24829685
    reference: chr 22
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000543438
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000543438.1:n.575-1283C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000473799
  ensembl transcript: ENST00000486108
  gene symbol: ADORA2A
  hgvsc: ENST00000486108.1:c.313G>A
  hgvsp: ENSP00000473799.1:p.Ala105Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000258555
  ensembl protein: ENSP00000351480
  ensembl transcript: ENST00000358654
  gene symbol: SPECC1L-ADORA2A
  hgvsc: ENST00000358654.2:c.*1448G>A
  variant of: http://identifiers.org/hgnc/49185
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000128271
  ensembl transcript: ENST00000496497
  gene symbol: ADORA2A
  hgvsc: ENST00000496497.1:n.100+5991G>A
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000178803
  ensembl transcript: ENST00000326341
  gene symbol: ADORA2A-AS1
  hgvsc: ENST00000326341.4:n.560-1283C>T
  variant of: http://identifiers.org/hgnc/37122
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000414802
  ensembl transcript: ENST00000444262
  gene symbol: ADORA2A
  hgvsc: ENST00000444262.2:c.313G>A
  hgvsp: ENSP00000414802.2:p.Ala105Thr
  variant of: http://identifiers.org/hgnc/263
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000128271
  ensembl protein: ENSP00000336630
  ensembl transcript: ENST00000337539
  gene symbol: ADORA2A
  hgvsc: ENST00000337539.7:c.313G>A
  hgvsp: ENSP00000336630.6:p.Ala105Thr
  variant of: http://identifiers.org/hgnc/263
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala105Thr
num of homozygotes: 0
reference allele: G

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

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

GenotypeDepth
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2834
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22898
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 2.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

FS
type: SiteQuality
SIO_000300: 7.16e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 4.8e0

DP
type: SiteQuality
SIO_000300: 3.7817e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.162e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

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

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

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

GenotypeQuality
all individuals: 884
bin: 9.75e1
variant carriers: 872

GenotypeQuality
all individuals: 101
bin: 7.25e1
variant carriers: 21

GenotypeQuality
all individuals: 607
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 991
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4180
bin: 6.25e1
variant carriers: 31

GenotypeQuality
all individuals: 372
bin: 6.75e1
variant carriers: 28

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1037
bin: 1.25e1
variant carriers: 19

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 29

GenotypeQuality
all individuals: 109
bin: 7.75e1
variant carriers: 32

GenotypeQuality
all individuals: 2193
bin: 1.75e1
variant carriers: 32

GenotypeQuality
all individuals: 16470
bin: 7.5e0
variant carriers: 9

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 40

GenotypeQuality
all individuals: 29539
bin: 2.25e1
variant carriers: 24

GenotypeQuality
all individuals: 1265
bin: 2.75e1
variant carriers: 16

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 26

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 38

GenotypeQuality
all individuals: 186
bin: 5.25e1
variant carriers: 24

GenotypeQuality
all individuals: 189
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1198
bin: 3.25e1
variant carriers: 16

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

South Asian
type: Population
allele count: 968
allele frequency: 1.430682825894177e-1
allele num: 6766
num of homozygotes: 54

East Asian
type: Population
allele count: 4
allele frequency: 4.366812227074236e-3
allele num: 916
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African
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Other
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Latino
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allele frequency: 1.230769230769231e-2
allele num: 650
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.390057361376673e-4
allele num: 8368
num of homozygotes: 0

InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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FS
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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 frequency: 1.077586206896552e-3
allele num: 1856
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.195028680688336e-4
allele num: 8368
num of homozygotes: 0

East Asian
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South Asian
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Other
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Latino
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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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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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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

East Asian
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European (Finnish)
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South Asian
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African
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Other
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European (Non-Finnish)
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allele frequency: 1.041232819658476e-4
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 528
num of homozygotes: 0

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

Latino
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Other
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European (Non-Finnish)
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allele num: 12456
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European (Finnish)
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African
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East Asian
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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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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European (Finnish)
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European (Non-Finnish)
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allele num: 13564
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Latino
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East Asian
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Other
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South Asian
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African
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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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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South Asian
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European (Non-Finnish)
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Latino
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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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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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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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South Asian
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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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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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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Latino
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South Asian
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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African
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Other
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MQRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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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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European (Finnish)
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South Asian
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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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African
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MQ
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InbreedingCoeff
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DP
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FS
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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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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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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East Asian
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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DP
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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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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Latino
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African
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VQSLOD
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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MQRankSum
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East Asian
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ClippingRankSum
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QD
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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
all individuals: 87
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.257545271629779e-4
allele num: 7952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5862
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7604
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51640
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
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SIO_000300: -2.89e-1

VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: -2.8e-3

DP
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SIO_000300: 1.101105e6

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 9.94e0

ClippingRankSum
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SIO_000300: -1.557e0

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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GenotypeQuality
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Other
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allele num: 744
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.394505647747873e-4
allele num: 14342
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.762227238525207e-4
allele num: 7974
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 3.208213025344883e-4
allele num: 6234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.720099698671925e-5
allele num: 53762
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.2e-3

MQ
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SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.138259e6

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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bin: 5.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14342
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 1.116029909601577e-4
allele num: 53762
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

Other
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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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.082e0

ClippingRankSum
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SIO_000300: 8.699999999999999e-2

InbreedingCoeff
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SIO_000300: 2.2e-3

ReadPosRankSum
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QD
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SIO_000300: 1.194e1

MQRankSum
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SIO_000300: 1.82e-1

BaseQRankSum
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SIO_000300: 2.86e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
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SIO_000300: 1.138259e6

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

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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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
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

Latino
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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 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
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num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.39463601532567e-4
allele num: 8352
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.171373e6

BaseQRankSum
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SIO_000300: 4.6e0

VQSLOD
type: SiteQuality
SIO_000300: -1.091e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.16e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6694
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.776640727712042e-5
allele num: 56286
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4878
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.181165e6

QD
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4878
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.776640727712042e-5
allele num: 56286
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
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DP
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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East Asian
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South Asian
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allele frequency: 6.523157208088715e-5
allele num: 15330
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Latino
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Other
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FS
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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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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East Asian
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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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InbreedingCoeff
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MQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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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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East Asian
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Latino
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European (Finnish)
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South Asian
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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Other
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East Asian
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MQ
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ClippingRankSum
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FS
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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DP
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InbreedingCoeff
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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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Other
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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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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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeDepth
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African
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East Asian
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MQ
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FS
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10328
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
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Other
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allele frequency: 0.0e0
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Finnish)
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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 frequency: 3.012864933265042e-5
allele num: 66382
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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InbreedingCoeff
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DP
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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MQ
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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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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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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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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
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South Asian
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African
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Other
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European (Non-Finnish)
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allele num: 66426
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East Asian
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FS
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQ
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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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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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Latino
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allele frequency: 0.0e0
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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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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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ClippingRankSum
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DP
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FS
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QD
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ReadPosRankSum
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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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variant carriers: 0

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

Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

East Asian
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allele frequency: 2.314814814814815e-4
allele num: 8640
num of homozygotes: 0

Latino
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South Asian
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allele frequency: 1.150678294573644e-3
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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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
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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 num: 66614
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East Asian
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South Asian
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Latino
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European (Finnish)
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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FS
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VQSLOD
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BaseQRankSum
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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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num of homozygotes: 0

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

East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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QD
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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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MQRankSum
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DP
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ClippingRankSum
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MQ
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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

European (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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European (Non-Finnish)
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.516762380107641e-5
allele num: 66518
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

Other
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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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East Asian
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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VQSLOD
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FS
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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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European (Non-Finnish)
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allele num: 66390
num of homozygotes: 0

European (Finnish)
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Latino
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African
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Other
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South Asian
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East Asian
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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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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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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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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East Asian
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European (Non-Finnish)
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African
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Other
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South Asian
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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South 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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MQRankSum
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DP
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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African
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South Asian
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MQ
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VQSLOD
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FS
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DP
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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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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GenotypeQuality
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African
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South Asian
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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QD
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MQRankSum
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InbreedingCoeff
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DP
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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African
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South Asian
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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East Asian
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African
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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FS
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.035e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.425e0

DP
type: SiteQuality
SIO_000300: 1.409728e6

VQSLOD
type: SiteQuality
SIO_000300: -2.805e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.72e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.410505e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

FS
type: SiteQuality
SIO_000300: 2.003e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 1.410703e6

QD
type: SiteQuality
SIO_000300: 9.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.410703e6

FS
type: SiteQuality
SIO_000300: 2.003e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

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

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.138e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

QD
type: SiteQuality
SIO_000300: 1.097e1

DP
type: SiteQuality
SIO_000300: 1.411108e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.0432e1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 47
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3767
bin: 6.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.912e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.411216e6

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.255e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

GenotypeQuality
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bin: 7.25e1
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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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.835e0

QD
type: SiteQuality
SIO_000300: 1.278e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.811e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.07e0

VQSLOD
type: SiteQuality
SIO_000300: -3.603e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.999e0

DP
type: SiteQuality
SIO_000300: 1.411045e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

FS
type: SiteQuality
SIO_000300: 2.384e0

QD
type: SiteQuality
SIO_000300: 1.184e1

DP
type: SiteQuality
SIO_000300: 1.411364e6

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 47
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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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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GenotypeQuality
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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: 556
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GenotypeQuality
all individuals: 21
bin: 2.75e1
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GenotypeQuality
all individuals: 210
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

FS
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.411308e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.112e0

QD
type: SiteQuality
SIO_000300: 1.033e1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.10014701029072e-4
allele num: 66662
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 1.794e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-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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bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.696e0

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.41282e6

FS
type: SiteQuality
SIO_000300: 6.663e0

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

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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bin: 4.25e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.662e0

VQSLOD
type: SiteQuality
SIO_000300: -3.425e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

FS
type: SiteQuality
SIO_000300: 2.683e1

DP
type: SiteQuality
SIO_000300: 1.412918e6

GenotypeQuality
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bin: 3.25e1
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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GenotypeQuality
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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: 21
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GenotypeQuality
all individuals: 55158
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999670036296008e-5
allele num: 66674
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.27e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

DP
type: SiteQuality
SIO_000300: 1.412843e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.825e0

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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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499640028797696e-5
allele num: 66672
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.852e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

DP
type: SiteQuality
SIO_000300: 1.413001e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.465e0

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.17e-2

QD
type: SiteQuality
SIO_000300: 1.392e1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
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: 0
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allele num: 16500
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 1.271970397779833e-3
allele num: 8648
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66610
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FS
type: SiteQuality
SIO_000300: 2.749e0

DP
type: SiteQuality
SIO_000300: 1.411563e6

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (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: 16430
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
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East Asian
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African
type: Population
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Other
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
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DP
type: SiteQuality
SIO_000300: 1.408692e6

VQSLOD
type: SiteQuality
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MQRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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QD
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