1-210334294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334294
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334294
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1653C>T
  hgvsp: ENST00000534859.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*257C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1632C>T
  hgvsp: ENST00000367019.1:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1461C>T
  hgvsp: ENST00000367015.1:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1575C>T
  hgvsp: ENST00000472886.1:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1461C>T
  hgvsp: ENST00000537238.1:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1767C>T
  hgvsp: ENST00000422431.1:c.1767C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1496C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1420C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn589Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

1-210334295-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334295
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334295
    reference: chr 1
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1462A>T
  hgvsp: ENSP00000437423.1:p.Ser488Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1462A>T
  hgvsp: ENSP00000355982.1:p.Ser488Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1654A>T
  hgvsp: ENSP00000442891.1:p.Ser552Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*258A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1768A>T
  hgvsp: ENSP00000389039.1:p.Ser590Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1633A>T
  hgvsp: ENSP00000355986.1:p.Ser545Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1576A>T
  hgvsp: ENSP00000418901.1:p.Ser526Cys
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1497A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1421A>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser590Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

1-210334302-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334302
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334299
    reference: chr 1
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1648_1650delGAA
  hgvsp: ENSP00000355986.1:p.Glu550del
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1783_1785delGAA
  hgvsp: ENSP00000389039.1:p.Glu595del
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1477_1479delGAA
  hgvsp: ENSP00000355982.1:p.Glu493del
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1512_1514delGAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1436_1438delGAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1477_1479delGAA
  hgvsp: ENSP00000437423.1:p.Glu493del
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*273_*275delGAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1591_1593delGAA
  hgvsp: ENSP00000418901.1:p.Glu531del
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1669_1671delGAA
  hgvsp: ENSP00000442891.1:p.Glu557del
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu595del
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: GAGA
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

1-210334335-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334335
    reference: chr 1
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1673A>G
  hgvsp: ENSP00000355986.1:p.Lys558Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1616A>G
  hgvsp: ENSP00000418901.1:p.Lys539Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1694A>G
  hgvsp: ENSP00000442891.1:p.Lys565Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1808A>G
  hgvsp: ENSP00000389039.1:p.Lys603Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1537A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*298A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1461A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1502A>G
  hgvsp: ENSP00000437423.1:p.Lys501Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1502A>G
  hgvsp: ENSP00000355982.1:p.Lys501Arg
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys603Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-210334350-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334350
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334350
    reference: chr 1
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*313A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1517A>T
  hgvsp: ENSP00000437423.1:p.Gln506Leu
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1709A>T
  hgvsp: ENSP00000442891.1:p.Gln570Leu
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1688A>T
  hgvsp: ENSP00000355986.1:p.Gln563Leu
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1823A>T
  hgvsp: ENSP00000389039.1:p.Gln608Leu
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1476A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1552A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1517A>T
  hgvsp: ENSP00000355982.1:p.Gln506Leu
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1631A>T
  hgvsp: ENSP00000418901.1:p.Gln544Leu
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln608Leu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

1-210334357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334357
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334357
    reference: chr 1
allele count: 5
allele frequency: 4.126161514466322e-5
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1830A>G
  hgvsp: ENST00000422431.1:c.1830A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1695A>G
  hgvsp: ENST00000367019.1:c.1695A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*320A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1638A>G
  hgvsp: ENST00000472886.1:c.1638A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1524A>G
  hgvsp: ENST00000537238.1:c.1524A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1559A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1483A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1716A>G
  hgvsp: ENST00000534859.1:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1524A>G
  hgvsp: ENST00000367015.1:c.1524A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val610Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

1-210334358-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334358
    reference: chr 1
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1525T>C
  hgvsp: ENSP00000355982.1:p.Cys509Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1639T>C
  hgvsp: ENSP00000418901.1:p.Cys547Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1831T>C
  hgvsp: ENSP00000389039.1:p.Cys611Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*321T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1525T>C
  hgvsp: ENSP00000437423.1:p.Cys509Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1717T>C
  hgvsp: ENSP00000442891.1:p.Cys573Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1560T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1696T>C
  hgvsp: ENSP00000355986.1:p.Cys566Arg
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1484T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16930
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys611Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-210334372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334372
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334372
    reference: chr 1
allele count: 8
allele frequency: 6.614412805503192e-5
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*335G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1731G>A
  hgvsp: ENST00000534859.1:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1710G>A
  hgvsp: ENST00000367019.1:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1653G>A
  hgvsp: ENST00000472886.1:c.1653G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1539G>A
  hgvsp: ENST00000537238.1:c.1539G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1845G>A
  hgvsp: ENST00000422431.1:c.1845G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1539G>A
  hgvsp: ENST00000367015.1:c.1539G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1498G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1574G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala615Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

1-210334378-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334378
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334378
    reference: chr 1
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1851A>G
  hgvsp: ENST00000422431.1:c.1851A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1737A>G
  hgvsp: ENST00000534859.1:c.1737A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1659A>G
  hgvsp: ENST00000472886.1:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1716A>G
  hgvsp: ENST00000367019.1:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1580A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1504A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1545A>G
  hgvsp: ENST00000367015.1:c.1545A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*341A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1545A>G
  hgvsp: ENST00000537238.1:c.1545A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu617Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-210334386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334386
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334386
    reference: chr 1
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*349G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1667G>A
  hgvsp: ENST00000472886.1:c.1667G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1512G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1859G>A
  hgvsp: ENST00000422431.1:c.1859G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1553G>A
  hgvsp: ENST00000367015.1:c.1553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1588G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1724G>A
  hgvsp: ENST00000367019.1:c.1724G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1553G>A
  hgvsp: ENST00000537238.1:c.1553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1745G>A
  hgvsp: ENST00000534859.1:c.1745G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ter620Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-210334386-GAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334386
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334384
    reference: chr 1
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*350_*351delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1589_1590delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.1668_*1delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.1746_*1delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.1554_*1delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.1860_*1delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1513_1514delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.1554_*1delAT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.1725_*1delAT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: coding sequence
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: GAT
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

1-210334390-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334390
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334390
    reference: chr 1
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*353A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1516A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*3A>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1592A>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-210334392-T-TTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334392
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334394
    reference: chr 1
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: TTC
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*355_*356insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1518_1519insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*5_*6insTC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1594_1595insTC
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

1-210334394-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334394
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334394
    reference: chr 1
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1596G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*357G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1520G>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

1-210334394-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334394
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334392
    reference: chr 1
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1597_1598delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*358_*359delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*8_*9delAA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1521_1522delAA
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: GAA
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-210334416-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334416
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334416
    reference: chr 1
allele count: 1
allele frequency: 8.427723840345199e-6
allele num: 118656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*379A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1618A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*29A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1542A>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16378
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-210334431-C-CTTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334431
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334435
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 112402
alternate allele: CTTTT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*394_*395insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1633_1634insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*44_*45insTTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1557_1558insTTTT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30321
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

1-210334441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334441
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334441
    reference: chr 1
allele count: 1
allele frequency: 9.4968565404851e-6
allele num: 105298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*404C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1567C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1643C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*54C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13177
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-210334456-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334456
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334456
    reference: chr 1
allele count: 1
allele frequency: 1.116295684400884e-5
allele num: 89582
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1582C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*419C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1658C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*69C>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

1-210334462-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334462
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334462
    reference: chr 1
allele count: 1
allele frequency: 1.209131360030954e-5
allele num: 82704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*425C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*75C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1588C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1664C>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11837
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-210334464-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334464
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334464
    reference: chr 1
allele count: 1
allele frequency: 1.254170115634485e-5
allele num: 79734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1590A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*427A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1666A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

1-210334476-GTTCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334476
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334472
    reference: chr 1
allele count: 1
allele frequency: 1.573910853689247e-5
allele num: 63536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1605_1608delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*442_*445delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*92_*95delCTTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1681_1684delCTTT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21132
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17002
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: GTTCT
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-210334477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334477
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334477
    reference: chr 1
allele count: 2
allele frequency: 3.134697971850412e-5
allele num: 63802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1679T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1603T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*440T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*90T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9811
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

1-210334481-TTGAAGAATCATATTCAAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334481
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334463
    reference: chr 1
allele count: 1
allele frequency: 1.705960626428742e-5
allele num: 58618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16291
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33530
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8745
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: TTGAAGAATCATATTCAAC
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum

1-210334483-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334483
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334482
    reference: chr 1
allele count: 1
allele frequency: 1.813894431344096e-5
allele num: 55130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1687delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*448delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*98delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1611delA
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15889
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: GA
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-210334497-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334497
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334497
    reference: chr 1
allele count: 1
allele frequency: 2.493765586034913e-5
allele num: 40100
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1699A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*460A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1623A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*110A>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17548
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

1-210334498-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334498
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334498
    reference: chr 1
allele count: 4
allele frequency: 1.041178614191265e-4
allele num: 38418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*461A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1700A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*111A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1624A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17650
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10933
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21313
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26500
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2051
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-210334505-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334505
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334505
    reference: chr 1
allele count: 1
allele frequency: 3.028834504482675e-5
allele num: 33016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1707A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*468A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1631A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*118A>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9033
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

1-210334565-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334565
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334565
    reference: chr 1
allele count: 1
allele frequency: 7.940289026520565e-5
allele num: 12594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1691T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*528T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1767T>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

1-210334630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334630
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334630
    reference: chr 1
allele count: 1
allele frequency: 8.787346221441125e-5
allele num: 11380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*593C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1832C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1756C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

1-210334665-GTTAATT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334665
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334659
    reference: chr 1
allele count: 2925
allele frequency: 2.64993658271426e-1
allele num: 11038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1875_1880delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1799_1804delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*636_*641delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*286_*291delTAATTT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 396
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 2.5e0
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 378
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 230
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.25e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 282
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 6.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.5e0
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 19
num of homozygotes: 393
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: GTTAATT
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/1-210334682-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334682
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334682
    reference: chr 1
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1808A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*645A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1884A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*295A>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  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: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-210334727-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334726
    reference: chr 1
allele count: 6
allele frequency: 5.661445555765239e-4
allele num: 10598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*695delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1858delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1934delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*345delA
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: TA
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

1-210334794-TTGAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334794
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334790
    reference: chr 1
allele count: 2
allele frequency: 1.864280387770321e-4
allele num: 10728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.1999_2002delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1923_1926delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*760_*763delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*410_*413delACTG
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.75e1
  variant carriers: 1
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: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TTGAC
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

1-210334847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334847
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334847
    reference: chr 1
allele count: 1
allele frequency: 9.295408068414203e-5
allele num: 10758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1973C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*810C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*460C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2049C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

1-210334852-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334852
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334852
    reference: chr 1
allele count: 5
allele frequency: 4.647704034207102e-4
allele num: 10758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.1978A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*815A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2054A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*465A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  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: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
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 quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-210334890-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334890
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334890
    reference: chr 1
allele count: 2
allele frequency: 1.859427296392711e-4
allele num: 10756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*853G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2016G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2092G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP

1-210334947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334947
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334947
    reference: chr 1
allele count: 3
allele frequency: 2.788104089219331e-4
allele num: 10760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2073G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*910G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2149G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*560G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-210334993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334993
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334993
    reference: chr 1
allele count: 2
allele frequency: 1.858736059479554e-4
allele num: 10760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*956A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2195A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2119A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*606A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

1-210334995-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210334995
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210334996
    reference: chr 1
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*959dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2122dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2198dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*609dupC
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  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: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

1-210335023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335023
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335023
    reference: chr 1
allele count: 1
allele frequency: 9.293680297397769e-5
allele num: 10760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*986T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2149T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2225T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*636T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ

1-210335027-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335027
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335026
    reference: chr 1
allele count: 1
allele frequency: 9.293680297397769e-5
allele num: 10760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2236delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*997delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*647delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2160delT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3448
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: AT
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-210335028-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335028
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335028
    reference: chr 1
allele count: 2814
allele frequency: 2.615727830451757e-1
allele num: 10758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2230T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2154T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*991T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*641T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 960
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.25e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 9.75e1
  variant carriers: 2430
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 380
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-210335060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335060
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335060
    reference: chr 1
allele count: 2
allele frequency: 1.858736059479554e-4
allele num: 10760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2262G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1023G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2186G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

1-210335065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335065
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335065
    reference: chr 1
allele count: 1
allele frequency: 9.293680297397769e-5
allele num: 10760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2267C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2191C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1028C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

1-210335066-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335066
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335066
    reference: chr 1
allele count: 2812
allele frequency: 2.612897230997956e-1
allele num: 10762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2192G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2268G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1029G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*679G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 9.75e1
  variant carriers: 1700
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 2.5e0
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 7.5e0
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 4
num of homozygotes: 380
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-210335080-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335080
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335080
    reference: chr 1
allele count: 1
allele frequency: 9.293680297397769e-5
allele num: 10760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1043G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2282G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2206G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*693G>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

1-210335102-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335102
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335102
    reference: chr 1
allele count: 9
allele frequency: 8.3674228337672e-4
allele num: 10756
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2228C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1065C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2304C>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.5e0
  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: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-210335136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335136
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335136
    reference: chr 1
allele count: 1
allele frequency: 9.300595238095238e-5
allele num: 10752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2262C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2338C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1099C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*749C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  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: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  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 depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-210335159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335159
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335159
    reference: chr 1
allele count: 1
allele frequency: 9.317927692881103e-5
allele num: 10732
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1122A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2285A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2361A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*772A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  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: 2888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

1-210335168-ATTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335168
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335165
    reference: chr 1
allele count: 22
allele frequency: 2.053004852556924e-3
allele num: 10716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1134_*1136delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2373_2375delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2297_2299delCTT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*784_*786delCTT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: ATTC
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

1-210335243-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335243
    reference: chr 1
allele count: 3
allele frequency: 2.836074872376631e-4
allele num: 10578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1206A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2369A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*856A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2445A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-210335256-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335256
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335256
    reference: chr 1
allele count: 1
allele frequency: 9.46611132146914e-5
allele num: 10564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2382G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2458G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1219G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  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: 463
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  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 quality: GenotypeQuality
  all individuals: 3752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

1-210335302-CGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335302
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335300
    reference: chr 1
allele count: 1
allele frequency: 9.45000945000945e-5
allele num: 10582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1266_*1267delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2429_2430delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2505_2506delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*916_*917delGA
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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 depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: CGA
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-210335337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335337
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335337
    reference: chr 1
allele count: 1
allele frequency: 9.46611132146914e-5
allele num: 10564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1300T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2539T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2463T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*950T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  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: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

1-210335425-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335425
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335425
    reference: chr 1
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2551A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1388A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*1038A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2627A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  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: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP

1-210335429-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335429
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335429
    reference: chr 1
allele count: 490
allele frequency: 5.019463224749027e-2
allele num: 9762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2631A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1392A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2555A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1042A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 2
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: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 2.25e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 2.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.75e1
  variant carriers: 450
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 16
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

1-210335499-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335499
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335499
    reference: chr 1
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1112T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2625T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1462T>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2701T>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
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: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

1-210335565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335565
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335565
    reference: chr 1
allele count: 1
allele frequency: 1.028594939312899e-4
allele num: 9722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2767G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355986
  ensembl transcript: ENST00000367019
  gene symbol: SYT14
  hgvsc: ENST00000367019.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1528G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1178G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2691G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  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: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum

1-210335589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335589
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335589
    reference: chr 1
allele count: 1
allele frequency: 1.028594939312899e-4
allele num: 9722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1552G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2791G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2715G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1202G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  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 depth: GenotypeDepth
  all individuals: 1397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-210335598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335598
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335598
    reference: chr 1
allele count: 1
allele frequency: 1.023122570083896e-4
allele num: 9774
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1211A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1211A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1211A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1561A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1211A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1211A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2800A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2724A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  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: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-210335619-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335619
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335619
    reference: chr 1
allele count: 1
allele frequency: 1.00928542591845e-4
allele num: 9908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1582G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1232G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1232G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1232G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1232G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1232G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2745G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2821G>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.25e1
  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 depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  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: 82
  bin: 3.25e1
  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: 392
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-210335644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335644
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335644
    reference: chr 1
allele count: 5
allele frequency: 4.837461300309598e-4
allele num: 10336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1257G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1257G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1607G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1257G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1257G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2846G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1257G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2770G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-210335644-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335644
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335644
    reference: chr 1
allele count: 7
allele frequency: 6.772445820433437e-4
allele num: 10336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1257G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2846G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1257G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2770G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1257G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1257G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1257G>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1607G>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

1-210335645-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335645
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335644
    reference: chr 1
allele count: 3
allele frequency: 2.901353965183752e-4
allele num: 10340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000418901
  ensembl transcript: ENST00000472886
  gene symbol: SYT14
  hgvsc: ENST00000472886.1:c.*1263delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1263delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2776delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1613delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2852delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1263delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1263delT
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1263delT
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AT
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-210335677-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335677
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335677
    reference: chr 1
allele count: 1
allele frequency: 9.503896597605019e-5
allele num: 10522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1290T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1290T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1640T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1290T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2803T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2879T>C
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1290T>C
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  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: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  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: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-210335680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335680
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335680
    reference: chr 1
allele count: 1
allele frequency: 9.496676163342829e-5
allele num: 10530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2806C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1293C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1293C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1643C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1293C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2882C>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1293C>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
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: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-210335685-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335685
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335685
    reference: chr 1
allele count: 1
allele frequency: 9.489466691971911e-5
allele num: 10538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2811G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2887G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1298G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1648G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1298G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1298G>T
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1298G>T
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

1-210335712-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335712
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335712
    reference: chr 1
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1325A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2838A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2914A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1325A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1675A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1325A>G
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1325A>G
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1093
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  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: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 2.75e1
  variant carriers: 1
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: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

1-210335724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 210335724
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 210335724
    reference: chr 1
allele count: 1
allele frequency: 9.912767644726408e-5
allele num: 10088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000437423
  ensembl transcript: ENST00000537238
  gene symbol: SYT14
  hgvsc: ENST00000537238.1:c.*1337G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000469604
  gene symbol: SYT14
  hgvsc: ENST00000469604.1:n.2850G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000389039
  ensembl transcript: ENST00000422431
  gene symbol: SYT14
  hgvsc: ENST00000422431.1:c.*1337G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000442891
  ensembl transcript: ENST00000534859
  gene symbol: SYT14
  hgvsc: ENST00000534859.1:c.*1337G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000445837
  ensembl transcript: ENST00000399639
  gene symbol: SYT14
  hgvsc: ENST00000399639.2:c.*1687G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143469
  ensembl transcript: ENST00000271745
  gene symbol: SYT14
  hgvsc: ENST00000271745.7:n.2926G>A
  variant of: http://identifiers.org/hgnc/23143
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000143469
  ensembl protein: ENSP00000355982
  ensembl transcript: ENST00000367015
  gene symbol: SYT14
  hgvsc: ENST00000367015.1:c.*1337G>A
  variant of: http://identifiers.org/hgnc/23143
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  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: 2
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.148e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.463e0

DP
type: SiteQuality
SIO_000300: 1.489046e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.673e0

QD
type: SiteQuality
SIO_000300: 1.126e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 318
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4233
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
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: 10402
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.317e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.489585e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 1.733e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 821
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GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.62e0

QD
type: SiteQuality
SIO_000300: 9.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

DP
type: SiteQuality
SIO_000300: 1.48903e6

MQ
type: SiteQuality
SIO_000300: 5.615e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.532e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
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bin: 9.25e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4225
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GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.487885e6

FS
type: SiteQuality
SIO_000300: 3.145e0

MQ
type: SiteQuality
SIO_000300: 5.867e1

VQSLOD
type: SiteQuality
SIO_000300: -9.284e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.68e-1

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 317
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variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 3.469e0

MQ
type: SiteQuality
SIO_000300: 4.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.203e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.596e1

VQSLOD
type: SiteQuality
SIO_000300: -2.242e0

DP
type: SiteQuality
SIO_000300: 1.48675e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 222
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.456022118541559e-4
allele num: 11574
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.43e0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 1.888e0

DP
type: SiteQuality
SIO_000300: 1.486091e6

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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 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: 906
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.31e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

FS
type: SiteQuality
SIO_000300: 1.821e0

MQRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

DP
type: SiteQuality
SIO_000300: 1.485484e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8636
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.867771857114664e-5
allele num: 10134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.008197459688316e-5
allele num: 66606
num of homozygotes: 0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.265e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 805
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 1.480955e6

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 2.372e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.89e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.478772e6

FS
type: SiteQuality
SIO_000300: 4.935e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.804e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6606
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.478772e6

FS
type: SiteQuality
SIO_000300: 4.935e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.804e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

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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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0569e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.477879e6

VQSLOD
type: SiteQuality
SIO_000300: -1.235e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.148e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.434e0

QD
type: SiteQuality
SIO_000300: 1.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-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
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.708e0

FS
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.931e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

QD
type: SiteQuality
SIO_000300: 6.86e0

MQ
type: SiteQuality
SIO_000300: 4.681e1

DP
type: SiteQuality
SIO_000300: 1.47728e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.4e1

DP
type: SiteQuality
SIO_000300: 1.476308e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.175e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.681e1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

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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bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.681e1

ClippingRankSum
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SIO_000300: 1.38e0

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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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.80126738250308e-5
allele num: 11362
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65322
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6068
num of homozygotes: 0

Other
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allele count: 1
allele frequency: 1.219512195121951e-3
allele num: 820
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

InbreedingCoeff
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SIO_000300: -2.4e-3

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 5.2e-1

DP
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SIO_000300: 1.257735e6

FS
type: SiteQuality
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QD
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SIO_000300: 1.41e1

VQSLOD
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MQRankSum
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SIO_000300: 1.23e0

BaseQRankSum
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SIO_000300: -4.243e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 48636
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.261034047919294e-4
allele num: 7930
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5338
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

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

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

BaseQRankSum
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SIO_000300: -2.083e0

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -6.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.235536081552356e-5
allele num: 44732
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7136
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6726
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13162
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

DP
type: SiteQuality
SIO_000300: 9.64334e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

MQRankSum
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FS
type: SiteQuality
SIO_000300: 5.693e0

QD
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MQ
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SIO_000300: 5.552e1

BaseQRankSum
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SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.332e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.94e-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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variant carriers: 0

Latino
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allele count: 1
allele frequency: 1.477978125923736e-4
allele num: 6766
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6496
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4784
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

VQSLOD
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SIO_000300: -1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.68e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.34397e5

MQRankSum
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SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.983471567515962e-5
allele num: 33518
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5058
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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.026e0

VQSLOD
type: SiteQuality
SIO_000300: -2.637e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

QD
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 5.521e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

DP
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SIO_000300: 7.82035e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5072
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3700
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5204
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 5.94106463878327e-5
allele num: 33664
num of homozygotes: 0

MQ
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 3270
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
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 3.266266004703423e-5
allele num: 30616
num of homozygotes: 0

ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
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QD
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DP
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 3.500175008750438e-5
allele num: 28570
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African
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MQ
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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South Asian
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African
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allele frequency: 3.107520198881293e-4
allele num: 3218
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
type: SiteQuality
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InbreedingCoeff
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MQ
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FS
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 2.10017851517379e-4
allele num: 19046
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

DP
type: SiteQuality
SIO_000300: 5.83259e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.61e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: -2.599e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.37e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2516
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.272738677706687e-5
allele num: 15942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1588
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.38962e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.35e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.26e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.554931016862545e-4
allele num: 3914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.683e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.51e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.063e-1

FS
type: SiteQuality
SIO_000300: 8.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.70501e5

GenotypeQuality
all individuals: 6
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.330849081714134e-4
allele num: 7514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.83e-2

QD
type: SiteQuality
SIO_000300: 1.104e1

FS
type: SiteQuality
SIO_000300: 4.544e0

VQSLOD
type: SiteQuality
SIO_000300: -1.126e0

MQ
type: SiteQuality
SIO_000300: 5.38e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e0

DP
type: SiteQuality
SIO_000300: 1.95867e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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variant carriers: 51

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2491

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 8

South Asian
type: Population
allele count: 1898
allele frequency: 2.530666666666667e-1
allele num: 7500
num of homozygotes: 248

African
type: Population
allele count: 25
allele frequency: 1.179245283018868e-1
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 864
allele frequency: 2.946793997271487e-1
allele num: 2932
num of homozygotes: 120

Other
type: Population
allele count: 40
allele frequency: 3.448275862068966e-1
allele num: 116
num of homozygotes: 9

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 31
allele frequency: 2.627118644067797e-1
allele num: 118
num of homozygotes: 5

East Asian
type: Population
allele count: 67
allele frequency: 4.1875e-1
allele num: 160
num of homozygotes: 11

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

DP
type: SiteQuality
SIO_000300: 1.90263e5

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.998e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.82e-2

MQ
type: SiteQuality
SIO_000300: 5.078e1

FS
type: SiteQuality
SIO_000300: 1.253e0

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.348435814455232e-4
allele num: 7416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.55811e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.39e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

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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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.351716680183834e-4
allele num: 7398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2672
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

African
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allele count: 5
allele frequency: 2.659574468085106e-2
allele num: 188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.027e1

FS
type: SiteQuality
SIO_000300: 4.282e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.87e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

DP
type: SiteQuality
SIO_000300: 1.4043e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 188
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South Asian
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allele count: 2
allele frequency: 2.668801708033093e-4
allele num: 7494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.49404e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.43e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 4.19e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

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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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.671071953010279e-4
allele num: 2724
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -4.937e0

ReadPosRankSum
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MQ
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DP
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SIO_000300: 1.50363e5

ClippingRankSum
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SIO_000300: -1.137e0

MQRankSum
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SIO_000300: 4.13e-1

QD
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InbreedingCoeff
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SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

FS
type: SiteQuality
SIO_000300: 1.103e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 5.330490405117271e-4
allele num: 7504
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 132
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Latino
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allele frequency: 0.0e0
allele num: 92
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Other
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allele frequency: 0.0e0
allele num: 118
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African
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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 frequency: 3.671071953010279e-4
allele num: 2724
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.5069e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

FS
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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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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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

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

European (Finnish)
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allele frequency: NaN
allele num: 0
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.981e1

FS
type: SiteQuality
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DP
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SIO_000300: 1.50454e5

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

South Asian
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allele frequency: 3.997867803837953e-4
allele num: 7504
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 118
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

FS
type: SiteQuality
SIO_000300: 3.89e-1

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.50811e5

BaseQRankSum
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SIO_000300: -3.658e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -2.43e-2

QD
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MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
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allele frequency: 2.665245202558635e-4
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-1

InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 1.0105e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: NaN
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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 (Non-Finnish)
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allele num: 2728
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Latino
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East Asian
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ClippingRankSum
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DP
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MQ
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 7504
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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Latino
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allele frequency: 0.0e0
allele num: 92
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European (Finnish)
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allele frequency: NaN
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.668378576669112e-4
allele num: 2726
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Other
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African
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Latino
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East Asian
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South Asian
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QD
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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variant carriers: 4

African
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num of homozygotes: 0

Latino
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allele frequency: 2.826086956521739e-1
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European (Finnish)
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num of homozygotes: 0

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