7-893242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893242
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893242
    reference: chr 7
allele count: 1
allele frequency: 8.820053273121769e-6
allele num: 113378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.941A>G
  hgvsp: ENSP00000413439.2:p.Gln314Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.795A>G
  hgvsp: ENSP00000406653.1:p.Gln266Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+20A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1359A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1001A>G
  hgvsp: ENSP00000374225.3:p.Gln334Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1361A>G
  hgvsp: ENSP00000384116.1:p.Gln454Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1025A>G
  hgvsp: ENSP00000409909.1:p.Gln342Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1001A>G
  hgvsp: ENSP00000392309.2:p.Gln334Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1817A>G
  hgvsp: ENSP00000388743.2:p.Gln606Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.490A>G
  hgvsp: ENSP00000406444.1:p.Gln164Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1250A>G
  hgvsp: ENSP00000384015.1:p.Gln417Arg
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1809A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26506
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9446
  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 quality: GenotypeQuality
hgvs: p.Gln417Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

7-893243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893243
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893243
    reference: chr 7
allele count: 6
allele frequency: 5.317546129712675e-5
allele num: 112834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1002G>A
  hgvsp: ENST00000389574.3:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1002G>A
  hgvsp: ENST00000425407.2:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1026G>A
  hgvsp: ENST00000429178.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1251G>A
  hgvsp: ENST00000401592.1:c.1251G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1360G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.942G>A
  hgvsp: ENST00000452783.2:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.796G>A
  hgvsp: ENST00000433212.1:c.796G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.491G>A
  hgvsp: ENST00000457861.1:c.491G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1362G>A
  hgvsp: ENST00000405266.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1810G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1818G>A
  hgvsp: ENST00000456758.2:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5735
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln417Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

7-893245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893245
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893245
    reference: chr 7
allele count: 1
allele frequency: 8.878156184523599e-6
allele num: 112636
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1253C>T
  hgvsp: ENSP00000384015.1:p.Pro418Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+23C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1812C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.493C>T
  hgvsp: ENSP00000406444.1:p.Pro165Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1028C>T
  hgvsp: ENSP00000409909.1:p.Pro343Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1362C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1820C>T
  hgvsp: ENSP00000388743.2:p.Pro607Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.798C>T
  hgvsp: ENSP00000406653.1:p.Pro267Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1004C>T
  hgvsp: ENSP00000392309.2:p.Pro335Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1004C>T
  hgvsp: ENSP00000374225.3:p.Pro335Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1364C>T
  hgvsp: ENSP00000384116.1:p.Pro455Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.944C>T
  hgvsp: ENSP00000413439.2:p.Pro315Leu
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro418Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

7-893246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893246
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893246
    reference: chr 7
allele count: 1
allele frequency: 8.896955461840959e-6
allele num: 112398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1254C>T
  hgvsp: ENST00000401592.1:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1029C>T
  hgvsp: ENST00000429178.1:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.494C>T
  hgvsp: ENST00000457861.1:c.494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1821C>T
  hgvsp: ENST00000456758.2:c.1821C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.799C>T
  hgvsp: ENST00000433212.1:c.799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1813C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+24C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.945C>T
  hgvsp: ENST00000452783.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1005C>T
  hgvsp: ENST00000425407.2:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1365C>T
  hgvsp: ENST00000405266.1:c.1365C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1005C>T
  hgvsp: ENST00000389574.3:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1363C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro418Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

7-893247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893247
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893247
    reference: chr 7
allele count: 2
allele frequency: 1.783007934385308e-5
allele num: 112170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1814C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1030C>T
  hgvsp: ENSP00000409909.1:p.Pro344Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.800C>T
  hgvsp: ENSP00000406653.1:p.Pro268Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.946C>T
  hgvsp: ENSP00000413439.2:p.Pro316Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1006C>T
  hgvsp: ENSP00000392309.2:p.Pro336Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1255C>T
  hgvsp: ENSP00000384015.1:p.Pro419Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1006C>T
  hgvsp: ENSP00000374225.3:p.Pro336Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.495C>T
  hgvsp: ENSP00000406444.1:p.Pro166Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1822C>T
  hgvsp: ENSP00000388743.2:p.Pro608Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+25C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1366C>T
  hgvsp: ENSP00000384116.1:p.Pro456Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1364C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro419Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

7-893248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893248
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893248
    reference: chr 7
allele count: 4
allele frequency: 3.575131386078438e-5
allele num: 111884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1815C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1365C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.496C>T
  hgvsp: ENSP00000406444.1:p.Pro166Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.801C>T
  hgvsp: ENSP00000406653.1:p.Pro268Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.947C>T
  hgvsp: ENSP00000413439.2:p.Pro316Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1256C>T
  hgvsp: ENSP00000384015.1:p.Pro419Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1367C>T
  hgvsp: ENSP00000384116.1:p.Pro456Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1031C>T
  hgvsp: ENSP00000409909.1:p.Pro344Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1823C>T
  hgvsp: ENSP00000388743.2:p.Pro608Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1007C>T
  hgvsp: ENSP00000374225.3:p.Pro336Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1007C>T
  hgvsp: ENSP00000392309.2:p.Pro336Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+26C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro419Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

7-893249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893249
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893249
    reference: chr 7
allele count: 9
allele frequency: 8.067552304630775e-5
allele num: 111558
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1257G>A
  hgvsp: ENST00000401592.1:c.1257G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1008G>A
  hgvsp: ENST00000389574.3:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1824G>A
  hgvsp: ENST00000456758.2:c.1824G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1816G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.948G>A
  hgvsp: ENST00000452783.2:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.497G>A
  hgvsp: ENST00000457861.1:c.497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1368G>A
  hgvsp: ENST00000405266.1:c.1368G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+27G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1032G>A
  hgvsp: ENST00000429178.1:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1008G>A
  hgvsp: ENST00000425407.2:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.802G>A
  hgvsp: ENST00000433212.1:c.802G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1366G>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12055
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  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: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro419Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-893249-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893249
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893249
    reference: chr 7
allele count: 2
allele frequency: 1.792789401029061e-5
allele num: 111558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.497G>C
  hgvsp: ENST00000457861.1:c.497G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.948G>C
  hgvsp: ENST00000452783.2:c.948G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1257G>C
  hgvsp: ENST00000401592.1:c.1257G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1008G>C
  hgvsp: ENST00000425407.2:c.1008G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1032G>C
  hgvsp: ENST00000429178.1:c.1032G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.802G>C
  hgvsp: ENST00000433212.1:c.802G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1008G>C
  hgvsp: ENST00000389574.3:c.1008G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1824G>C
  hgvsp: ENST00000456758.2:c.1824G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1816G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1368G>C
  hgvsp: ENST00000405266.1:c.1368G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1366G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+27G>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12055
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro419Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-893254-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893254
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893255
    reference: chr 7
allele count: 1
allele frequency: 9.041918333393613e-6
allele num: 110596
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+34dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+1dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+1dupG
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

7-893259-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893259
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893259
    reference: chr 7
allele count: 6
allele frequency: 5.51460451094649e-5
allele num: 108802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+4G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+37G>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19244
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10259
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1263+4G>C
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

7-893262-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893262
    reference: chr 7
allele count: 4
allele frequency: 3.693648770938372e-5
allele num: 108294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+7G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+40G>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18263
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1263+7G>T
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

7-893267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893267
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893267
    reference: chr 7
allele count: 6
allele frequency: 5.599417660563302e-5
allele num: 107154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+45C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+12C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+12C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9939
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-893268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893268
    reference: chr 7
allele count: 39
allele frequency: 3.664311485267589e-4
allele num: 106432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+46G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+13G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+13G>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15151
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15600
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/7-893273-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893273
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893272
    reference: chr 7
allele count: 1
allele frequency: 9.482807669694844e-6
allele num: 105454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+53delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+20delC
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+20delC
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: AC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-893275-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893275
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893275
    reference: chr 7
allele count: 1
allele frequency: 9.512032721392561e-6
allele num: 105130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+53C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+20C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8840
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-893283-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893283
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893283
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 103410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+61A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+28A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+28A>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

7-893289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893289
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893289
    reference: chr 7
allele count: 1
allele frequency: 1.000780608874922e-5
allele num: 99922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+67A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+34A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18167
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

7-893292-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893292
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893292
    reference: chr 7
allele count: 2
allele frequency: 2.039110132338248e-5
allele num: 98082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+70C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+37C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+37C>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8178
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-893295-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893295
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893295
    reference: chr 7
allele count: 1
allele frequency: 1.037021673752982e-5
allele num: 96430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+73A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+40A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+40A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8214
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

7-893296-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893296
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893296
    reference: chr 7
allele count: 6
allele frequency: 6.283906914392241e-5
allele num: 95482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+74C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+41C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+41C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17663
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14681
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-893297-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893297
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893297
    reference: chr 7
allele count: 44161
allele frequency: 4.678072033898305e-1
allele num: 94400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+75G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+42G>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+42G>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 2.75e1
  variant carriers: 3253
genotype depth: GenotypeDepth
  all individuals: 17653
  bin: 1.25e1
  variant carriers: 11045
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 2.5e0
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 474
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.25e1
  variant carriers: 6477
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 3.25e1
  variant carriers: 1678
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 924
genotype depth: GenotypeDepth
  all individuals: 14992
  bin: 1.75e1
  variant carriers: 10715
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 7.5e0
  variant carriers: 4615
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 222
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 9824
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

7-893298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893298
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893298
    reference: chr 7
allele count: 3
allele frequency: 3.385087560931576e-5
allele num: 88624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+76C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+43C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21048
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13233
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

7-893299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 893299
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 893299
    reference: chr 7
allele count: 3
allele frequency: 3.491376300537672e-5
allele num: 85926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.808+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.954+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1038+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.657+77G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1374+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1822+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1372+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1014+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1263+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1014+44G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1830+44G>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20275
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13219
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

7-894508-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894508
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894508
    reference: chr 7
allele count: 1
allele frequency: 8.401243384020834e-6
allele num: 119030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-49T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1253T>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

7-894512-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894512
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894513
    reference: chr 7
allele count: 1
allele frequency: 8.398562166157153e-6
allele num: 119068
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1258dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-44dupG
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-44dupG
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17111
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

7-894514-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894514
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894514
    reference: chr 7
allele count: 1
allele frequency: 8.383635144198524e-6
allele num: 119280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1259C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-43C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-43C>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-894514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894514
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894514
    reference: chr 7
allele count: 1
allele frequency: 8.383635144198524e-6
allele num: 119280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1259C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-43C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-43C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-894517-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894517
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894517
    reference: chr 7
allele count: 1
allele frequency: 8.371142995864656e-6
allele num: 119458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-40A>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1262A>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7375
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-894523-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894523
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894523
    reference: chr 7
allele count: 1
allele frequency: 8.364421098415779e-6
allele num: 119554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-34C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1268C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-34C>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21725
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

7-894525-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894525
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894525
    reference: chr 7
allele count: 1
allele frequency: 8.358408559010364e-6
allele num: 119640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-32C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1270C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-32C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-894526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894526
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894526
    reference: chr 7
allele count: 1
allele frequency: 8.356732183446986e-6
allele num: 119664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1271C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-31C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-31C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

7-894527-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894527
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894527
    reference: chr 7
allele count: 2
allele frequency: 1.6703135178473e-5
allele num: 119738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1272A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-30A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-30A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

7-894534-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894534
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894534
    reference: chr 7
allele count: 117
allele frequency: 9.752438109527382e-4
allele num: 119970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1279G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-23G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-23G>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22681
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 23393
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

7-894538-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894538
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894538
    reference: chr 7
allele count: 1
allele frequency: 8.326117364950376e-6
allele num: 120104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1283A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-19A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-19A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

7-894543-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894543
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894543
    reference: chr 7
allele count: 18
allele frequency: 1.497529077022912e-4
allele num: 120198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1288T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-14T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-14T>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23534
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23211
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

7-894543-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894543
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894541
    reference: chr 7
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-10_1015-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-10_1015-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-10_1039-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-10_809-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-10_658-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-10_1831-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-10_1823-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-10_955-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-10_1264-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-10_1375-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-10_1373-9delCT
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1292_503+1293delCT
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: TTC
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

7-894547-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894547
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894547
    reference: chr 7
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1292C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-10C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-10C>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-894551-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894551
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894551
    reference: chr 7
allele count: 77
allele frequency: 6.398324802233597e-4
allele num: 120344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1296C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-6C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-6C>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23638
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 23355
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7696
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: c.1264-6C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-894554-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894554
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894554
    reference: chr 7
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1831-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1264-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.955-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1015-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1015-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1299A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1373-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1039-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.658-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.809-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1375-3A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1823-3A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23681
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1264-3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

7-894558-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894558
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894558
    reference: chr 7
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1016C>G
  hgvsp: ENSP00000392309.2:p.Thr339Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1374C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.659C>G
  hgvsp: ENSP00000389313.2:p.Thr220Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1016C>G
  hgvsp: ENSP00000374225.3:p.Thr339Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1040C>G
  hgvsp: ENSP00000409909.1:p.Thr347Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1265C>G
  hgvsp: ENSP00000384015.1:p.Thr422Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.956C>G
  hgvsp: ENSP00000413439.2:p.Thr319Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1376C>G
  hgvsp: ENSP00000384116.1:p.Thr459Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1832C>G
  hgvsp: ENSP00000388743.2:p.Thr611Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1824C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1303C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.810C>G
  hgvsp: ENSP00000406653.1:p.Thr271Ser
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr422Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

7-894563-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894563
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894563
    reference: chr 7
allele count: 3
allele frequency: 2.490411914130597e-5
allele num: 120462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1045T>C
  hgvsp: ENSP00000409909.1:p.Phe349Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1379T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.961T>C
  hgvsp: ENSP00000413439.2:p.Phe321Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.815T>C
  hgvsp: ENSP00000406653.1:p.Phe273Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1021T>C
  hgvsp: ENSP00000392309.2:p.Phe341Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1837T>C
  hgvsp: ENSP00000388743.2:p.Phe613Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1270T>C
  hgvsp: ENSP00000384015.1:p.Phe424Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1021T>C
  hgvsp: ENSP00000374225.3:p.Phe341Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1381T>C
  hgvsp: ENSP00000384116.1:p.Phe461Leu
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1308T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1829T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.664T>C
  hgvsp: ENSP00000389313.2:p.Phe222Leu
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe424Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

7-894563-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894563
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894563
    reference: chr 7
allele count: 2
allele frequency: 1.660274609420398e-5
allele num: 120462
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1308T>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1381T>A
  hgvsp: ENSP00000384116.1:p.Phe461Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.664T>A
  hgvsp: ENSP00000389313.2:p.Phe222Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1021T>A
  hgvsp: ENSP00000392309.2:p.Phe341Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1379T>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1270T>A
  hgvsp: ENSP00000384015.1:p.Phe424Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1021T>A
  hgvsp: ENSP00000374225.3:p.Phe341Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1837T>A
  hgvsp: ENSP00000388743.2:p.Phe613Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1045T>A
  hgvsp: ENSP00000409909.1:p.Phe349Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.815T>A
  hgvsp: ENSP00000406653.1:p.Phe273Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.961T>A
  hgvsp: ENSP00000413439.2:p.Phe321Ile
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1829T>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe424Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

7-894564-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894564
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894564
    reference: chr 7
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1382T>G
  hgvsp: ENSP00000384116.1:p.Phe461Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1022T>G
  hgvsp: ENSP00000374225.3:p.Phe341Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1046T>G
  hgvsp: ENSP00000409909.1:p.Phe349Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1022T>G
  hgvsp: ENSP00000392309.2:p.Phe341Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.665T>G
  hgvsp: ENSP00000389313.2:p.Phe222Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1271T>G
  hgvsp: ENSP00000384015.1:p.Phe424Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.962T>G
  hgvsp: ENSP00000413439.2:p.Phe321Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1838T>G
  hgvsp: ENSP00000388743.2:p.Phe613Cys
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1830T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1380T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1309T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.816T>G
  hgvsp: ENSP00000406653.1:p.Phe273Cys
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe424Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

7-894580-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894580
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894580
    reference: chr 7
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1062A>G
  hgvsp: ENST00000429178.1:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1854A>G
  hgvsp: ENST00000456758.2:c.1854A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1396A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.832A>G
  hgvsp: ENST00000433212.1:c.832A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1038A>G
  hgvsp: ENST00000425407.2:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1038A>G
  hgvsp: ENST00000389574.3:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1287A>G
  hgvsp: ENST00000401592.1:c.1287A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1846A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.681A>G
  hgvsp: ENST00000413514.2:c.681A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1325A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.978A>G
  hgvsp: ENST00000452783.2:c.978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1398A>G
  hgvsp: ENST00000405266.1:c.1398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln429Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-894583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894583
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894583
    reference: chr 7
allele count: 10
allele frequency: 8.295863682367971e-5
allele num: 120542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1065A>G
  hgvsp: ENST00000429178.1:c.1065A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1849A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1401A>G
  hgvsp: ENST00000405266.1:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1328A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1857A>G
  hgvsp: ENST00000456758.2:c.1857A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1290A>G
  hgvsp: ENST00000401592.1:c.1290A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1399A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.981A>G
  hgvsp: ENST00000452783.2:c.981A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1041A>G
  hgvsp: ENST00000389574.3:c.1041A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.684A>G
  hgvsp: ENST00000413514.2:c.684A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.835A>G
  hgvsp: ENST00000433212.1:c.835A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1041A>G
  hgvsp: ENST00000425407.2:c.1041A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu430Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

7-894589-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894589
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894589
    reference: chr 7
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.690A>G
  hgvsp: ENST00000413514.2:c.690A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1334A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1407A>G
  hgvsp: ENST00000405266.1:c.1407A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1071A>G
  hgvsp: ENST00000429178.1:c.1071A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1863A>G
  hgvsp: ENST00000456758.2:c.1863A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.841A>G
  hgvsp: ENST00000433212.1:c.841A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1855A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1047A>G
  hgvsp: ENST00000425407.2:c.1047A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1047A>G
  hgvsp: ENST00000389574.3:c.1047A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1296A>G
  hgvsp: ENST00000401592.1:c.1296A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1405A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.987A>G
  hgvsp: ENST00000452783.2:c.987A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu432Glu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

7-894591-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894591
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894591
    reference: chr 7
allele count: 4
allele frequency: 3.318180309918041e-5
allele num: 120548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1407T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1049T>G
  hgvsp: ENSP00000374225.3:p.Val350Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1073T>G
  hgvsp: ENSP00000409909.1:p.Val358Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1049T>G
  hgvsp: ENSP00000392309.2:p.Val350Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.843T>G
  hgvsp: ENSP00000406653.1:p.Val282Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1865T>G
  hgvsp: ENSP00000388743.2:p.Val622Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.692T>G
  hgvsp: ENSP00000389313.2:p.Val231Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.989T>G
  hgvsp: ENSP00000413439.2:p.Val330Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1857T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1298T>G
  hgvsp: ENSP00000384015.1:p.Val433Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1409T>G
  hgvsp: ENSP00000384116.1:p.Val470Gly
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1336T>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val433Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-894594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894594
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894594
    reference: chr 7
allele count: 2
allele frequency: 1.659200265472042e-5
allele num: 120540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.846G>A
  hgvsp: ENSP00000406653.1:p.Arg283His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1860G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1076G>A
  hgvsp: ENSP00000409909.1:p.Arg359His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1052G>A
  hgvsp: ENSP00000392309.2:p.Arg351His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1868G>A
  hgvsp: ENSP00000388743.2:p.Arg623His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1412G>A
  hgvsp: ENSP00000384116.1:p.Arg471His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.695G>A
  hgvsp: ENSP00000389313.2:p.Arg232His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1052G>A
  hgvsp: ENSP00000374225.3:p.Arg351His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1301G>A
  hgvsp: ENSP00000384015.1:p.Arg434His
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1410G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1339G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.992G>A
  hgvsp: ENSP00000413439.2:p.Arg331His
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg434His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

7-894605-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894605
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894605
    reference: chr 7
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1087T>G
  hgvsp: ENSP00000409909.1:p.Leu363Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.706T>G
  hgvsp: ENSP00000389313.2:p.Leu236Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1879T>G
  hgvsp: ENSP00000388743.2:p.Leu627Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.857T>G
  hgvsp: ENSP00000406653.1:p.Leu287Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1423T>G
  hgvsp: ENSP00000384116.1:p.Leu475Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1063T>G
  hgvsp: ENSP00000374225.3:p.Leu355Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1003T>G
  hgvsp: ENSP00000413439.2:p.Leu335Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1350T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1421T>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1312T>G
  hgvsp: ENSP00000384015.1:p.Leu438Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1063T>G
  hgvsp: ENSP00000392309.2:p.Leu355Val
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1871T>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu438Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-894606-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894606
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894606
    reference: chr 7
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1313T>C
  hgvsp: ENSP00000384015.1:p.Leu438Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1064T>C
  hgvsp: ENSP00000374225.3:p.Leu355Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1424T>C
  hgvsp: ENSP00000384116.1:p.Leu475Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.858T>C
  hgvsp: ENSP00000406653.1:p.Leu287Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1088T>C
  hgvsp: ENSP00000409909.1:p.Leu363Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1064T>C
  hgvsp: ENSP00000392309.2:p.Leu355Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1880T>C
  hgvsp: ENSP00000388743.2:p.Leu627Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.707T>C
  hgvsp: ENSP00000389313.2:p.Leu236Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1004T>C
  hgvsp: ENSP00000413439.2:p.Leu335Ser
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1422T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1872T>C
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1351T>C
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu438Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

7-894619-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894619
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894619
    reference: chr 7
allele count: 8
allele frequency: 6.645732608948479e-5
allele num: 120378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1326G>T
  hgvsp: ENST00000401592.1:c.1326G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1437G>T
  hgvsp: ENST00000405266.1:c.1437G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.871G>T
  hgvsp: ENST00000433212.1:c.871G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1893G>T
  hgvsp: ENST00000456758.2:c.1893G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.720G>T
  hgvsp: ENST00000413514.2:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1077G>T
  hgvsp: ENST00000425407.2:c.1077G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1101G>T
  hgvsp: ENST00000429178.1:c.1101G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.503+1364G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1435G>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1017G>T
  hgvsp: ENST00000452783.2:c.1017G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1077G>T
  hgvsp: ENST00000389574.3:c.1077G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1885G>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu442Leu
num of homozygotes: 1
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

7-894628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894628
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894628
    reference: chr 7
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.729G>A
  hgvsp: ENST00000413514.2:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1446G>A
  hgvsp: ENST00000405266.1:c.1446G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1444G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1902G>A
  hgvsp: ENST00000456758.2:c.1902G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1367G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1086G>A
  hgvsp: ENST00000425407.2:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1086G>A
  hgvsp: ENST00000389574.3:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.880G>A
  hgvsp: ENST00000433212.1:c.880G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1110G>A
  hgvsp: ENST00000429178.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1026G>A
  hgvsp: ENST00000452783.2:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1894G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1335G>A
  hgvsp: ENST00000401592.1:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu445Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-894658-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894658
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894658
    reference: chr 7
allele count: 36
allele frequency: 3.117584910889031e-4
allele num: 115474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1337C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+15C>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+15C>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21523
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

7-894658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894658
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894658
    reference: chr 7
allele count: 24
allele frequency: 2.078389940592687e-4
allele num: 115474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1337C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+15C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+15C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21523
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/7-894659-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894659
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894659
    reference: chr 7
allele count: 1
allele frequency: 8.696408383337681e-6
allele num: 114990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+16C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1336C>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+16C>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

7-894659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894659
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894659
    reference: chr 7
allele count: 2
allele frequency: 1.739281676667536e-5
allele num: 114990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1336C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+16C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+16C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

7-894663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894663
    reference: chr 7
allele count: 2
allele frequency: 1.761369641032867e-5
allele num: 113548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1332C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+20C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+20C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS

7-894664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894664
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894664
    reference: chr 7
allele count: 38
allele frequency: 3.357127712205809e-4
allele num: 113192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1331G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+21G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+21G>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19362
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

7-894665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894665
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894665
    reference: chr 7
allele count: 1
allele frequency: 8.863990923273295e-6
allele num: 112816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1330C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+22C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+22C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD

7-894672-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894672
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894672
    reference: chr 7
allele count: 9
allele frequency: 8.09949783113447e-5
allele num: 111118
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+29A>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1323A>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6168
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15092
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

7-894676-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894676
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894673
    reference: chr 7
allele count: 2
allele frequency: 1.82278850185013e-5
allele num: 109722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+36_1041+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+36_744+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+36_1909+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+36_1350+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+36_895+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+36_1459+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+36_1461+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1316_504-1314delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+36_1125+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+36_1917+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+36_1101+38delAAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+36_1101+38delAAA
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7664
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: TAAA
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-894677-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894677
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894677
    reference: chr 7
allele count: 7
allele frequency: 6.38022494850247e-5
allele num: 109714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1318A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+34A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+34A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17541
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9454
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

7-894679-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894679
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894676
    reference: chr 7
allele count: 1
allele frequency: 9.232587340276238e-6
allele num: 108312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+39_1101+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+39_1350+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1313_504-1311delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+39_1461+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+39_1041+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+39_895+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+39_744+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+39_1909+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+39_1917+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+39_1125+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+39_1459+41delGAA
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+39_1101+41delGAA
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: AAAG
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

7-894682-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894682
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894682
    reference: chr 7
allele count: 1
allele frequency: 9.294371328723325e-6
allele num: 107592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1313G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+39G>A
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+39G>A
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9076
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

7-894691-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894691
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894691
    reference: chr 7
allele count: 1
allele frequency: 9.724788485850432e-6
allele num: 102830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1304C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+48C>T
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+48C>T
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15958
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-894693-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 894693
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 894693
    reference: chr 7
allele count: 1
allele frequency: 9.849111610132765e-6
allele num: 101532
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1350+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.895+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1101+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1909+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1461+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1041+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.744+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1101+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1125+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1459+50A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-1302A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1917+50A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9624
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

7-895949-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 895949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 895949
    reference: chr 7
allele count: 2
allele frequency: 1.66245511371193e-5
allele num: 120304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000409909
  ensembl transcript: ENST00000429178
  gene symbol: SUN1
  hgvsc: ENST00000429178.1:c.1126-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000413171
  gene symbol: SUN1
  hgvsc: ENST00000413171.2:n.1910-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000413439
  ensembl transcript: ENST00000452783
  gene symbol: SUN1
  hgvsc: ENST00000452783.2:c.1042-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406444
  ensembl transcript: ENST00000457861
  gene symbol: SUN1
  hgvsc: ENST00000457861.1:c.504-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000406653
  ensembl transcript: ENST00000433212
  gene symbol: SUN1
  hgvsc: ENST00000433212.1:c.896-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000388743
  ensembl transcript: ENST00000456758
  gene symbol: SUN1
  hgvsc: ENST00000456758.2:c.1918-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384116
  ensembl transcript: ENST00000405266
  gene symbol: SUN1
  hgvsc: ENST00000405266.1:c.1462-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000389313
  ensembl transcript: ENST00000413514
  gene symbol: SUN1
  hgvsc: ENST00000413514.2:c.745-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl transcript: ENST00000475971
  gene symbol: SUN1
  hgvsc: ENST00000475971.1:n.1460-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000384015
  ensembl transcript: ENST00000401592
  gene symbol: SUN1
  hgvsc: ENST00000401592.1:c.1351-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000392309
  ensembl transcript: ENST00000425407
  gene symbol: SUN1
  hgvsc: ENST00000425407.2:c.1102-46A>G
  variant of: http://identifiers.org/hgnc/18587
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000164828
  ensembl protein: ENSP00000374225
  ensembl transcript: ENST00000389574
  gene symbol: SUN1
  hgvsc: ENST00000389574.3:c.1102-46A>G
  variant of: http://identifiers.org/hgnc/18587
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 3009
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7191
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.603900686469494e-5
allele num: 62348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.48e-1

FS
type: SiteQuality
SIO_000300: 1.155e0

DP
type: SiteQuality
SIO_000300: 1.480414e6

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 5.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.594e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeDepth
all individuals: 9211
bin: 3.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.342143906020558e-4
allele num: 8172
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
type: SiteQuality
SIO_000300: 1.189e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

FS
type: SiteQuality
SIO_000300: 7.63e-1

DP
type: SiteQuality
SIO_000300: 1.465959e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.692e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34982
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614569878584345e-5
allele num: 61936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
type: SiteQuality
SIO_000300: 1.455148e6

VQSLOD
type: SiteQuality
SIO_000300: -3.12e-2

FS
type: SiteQuality
SIO_000300: 3.424e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.79e-1

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

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

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 739
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7037
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.617704154264268e-5
allele num: 61816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.448364e6

FS
type: SiteQuality
SIO_000300: 2.655e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.064e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 2.856e1

GenotypeDepth
all individuals: 8612
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7341
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.621218507830485e-5
allele num: 61682
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.175e1

FS
type: SiteQuality
SIO_000300: 2.908e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 6.97e-1

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 1.439813e6

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10924
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.502584777449036e-5
allele num: 61514
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5772
num of homozygotes: 0

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: 8110
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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DP
type: SiteQuality
SIO_000300: 1.432469e6

QD
type: SiteQuality
SIO_000300: 2.695e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 9.191176470588235e-5
allele num: 10880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.892687063735403e-5
allele num: 61316
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 6.181998021760633e-4
allele num: 8088
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5770
num of homozygotes: 0

African
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allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.417391e6

VQSLOD
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QD
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MQRankSum
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FS
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MQ
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SIO_000300: 5.938e1

InbreedingCoeff
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SIO_000300: 4.2e-3

BaseQRankSum
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SIO_000300: -1.621e0

ClippingRankSum
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SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.472799208704253e-4
allele num: 8088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5770
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

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
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FS
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QD
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MQRankSum
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MQ
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SIO_000300: 5.938e1

ReadPosRankSum
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DP
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SIO_000300: 1.417391e6

BaseQRankSum
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SIO_000300: -1.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 303
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8022
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.177024482109228e-4
allele num: 8496
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16022
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ClippingRankSum
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SIO_000300: 1.26e0

BaseQRankSum
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SIO_000300: 1.58e0

MQRankSum
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SIO_000300: 1.17e0

ReadPosRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 3.05e0

DP
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SIO_000300: 1.37624e6

MQ
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SIO_000300: 6.022e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10550
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 1.00351229302559e-4
allele num: 59790
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15834
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.246882793017456e-3
allele num: 802
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European (Finnish)
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allele count: 1
allele frequency: 1.812250815512867e-4
allele num: 5518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.362700921380053e-5
allele num: 59476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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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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QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 1
allele frequency: 6.350819255683983e-5
allele num: 15746
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.451581269919098e-4
allele num: 8158
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 5.094243504839531e-5
allele num: 58890
num of homozygotes: 0

East Asian
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Other
type: Population
allele count: 0
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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African
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East Asian
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Latino
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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Other
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African
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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South Asian
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Other
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European (Finnish)
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Latino
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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South Asian
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European (Non-Finnish)
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VQSLOD
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DP
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FS
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1599
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.772314777190844e-5
allele num: 14766
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.525623928367309e-5
allele num: 52490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
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SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 9.88246e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1006

GenotypeQuality
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bin: 5.75e1
variant carriers: 675

GenotypeQuality
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bin: 1.25e1
variant carriers: 350

GenotypeQuality
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bin: 1.75e1
variant carriers: 674

GenotypeQuality
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bin: 9.25e1
variant carriers: 667

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 1459

GenotypeQuality
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variant carriers: 419

GenotypeQuality
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variant carriers: 804

GenotypeQuality
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variant carriers: 750

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1297

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 934

GenotypeQuality
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variant carriers: 1241

GenotypeQuality
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bin: 2.75e1
variant carriers: 662

GenotypeQuality
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variant carriers: 619

GenotypeQuality
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variant carriers: 25149

GenotypeQuality
all individuals: 603
bin: 8.75e1
variant carriers: 564

African
type: Population
allele count: 3441
allele frequency: 4.733149931224209e-1
allele num: 7270
num of homozygotes: 765

European (Non-Finnish)
type: Population
allele count: 23295
allele frequency: 4.498841251448435e-1
allele num: 51780
num of homozygotes: 4882

South Asian
type: Population
allele count: 6689
allele frequency: 4.525098092274388e-1
allele num: 14782
num of homozygotes: 1505

Latino
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allele count: 3611
allele frequency: 4.216487622606259e-1
allele num: 8564
num of homozygotes: 650

East Asian
type: Population
allele count: 4434
allele frequency: 6.598214285714286e-1
allele num: 6720
num of homozygotes: 1398

European (Finnish)
type: Population
allele count: 2368
allele frequency: 5.172564438619485e-1
allele num: 4578
num of homozygotes: 555

Other
type: Population
allele count: 323
allele frequency: 4.575070821529745e-1
allele num: 706
num of homozygotes: 69

QD
type: SiteQuality
SIO_000300: 2.2e1

MQRankSum
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SIO_000300: 3.6e-2

ClippingRankSum
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SIO_000300: -1.16e-1

VQSLOD
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 2.54e-2

ReadPosRankSum
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SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 9.82362e5

BaseQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3065
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 143
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48940
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.232437761893024e-4
allele num: 8114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.063144511936714e-5
allele num: 14158
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.70299727520436e-4
allele num: 5872
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.565e1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 3.77e-1

BaseQRankSum
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SIO_000300: 2.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 8.61176e5

GenotypeDepth
all individuals: 3258
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 428
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GenotypeQuality
all individuals: 399
bin: 8.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.152080344332855e-4
allele num: 13940
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.563e1

VQSLOD
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SIO_000300: 2.68e0

ReadPosRankSum
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SIO_000300: 2.12e-1

MQRankSum
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SIO_000300: 5.73e-1

ClippingRankSum
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SIO_000300: -4.37e-1

BaseQRankSum
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SIO_000300: -1.001e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

DP
type: SiteQuality
SIO_000300: 8.48737e5

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 968
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GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521931026085898e-5
allele num: 65706
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e0

DP
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.932e1

ReadPosRankSum
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SIO_000300: 3.8e-2

MQRankSum
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QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521931026085898e-5
allele num: 65706
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 3.39e-1

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.14e1

DP
type: SiteQuality
SIO_000300: 1.615064e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2897
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

InbreedingCoeff
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QD
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.624481e6

GenotypeDepth
all individuals: 55
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
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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
all individuals: 1522
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.736676568233443e-5
allele num: 11446
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65806
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.02e0

ReadPosRankSum
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SIO_000300: 7.4e-2

VQSLOD
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.7e-3

FS
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SIO_000300: 3.522e0

BaseQRankSum
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SIO_000300: 4.04e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

African
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allele frequency: 1.034340091021928e-4
allele num: 9668
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 3.11e-1

BaseQRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.89e-1

DP
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GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65990
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Latino
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South Asian
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allele num: 16364
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Other
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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FS
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MQ
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SIO_000300: 5.906e1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66050
num of homozygotes: 0

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

Latino
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allele frequency: 8.722958827634333e-5
allele num: 11464
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MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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SIO_000300: 6.463e0

ReadPosRankSum
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SIO_000300: -4.15e-1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
type: Population
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allele frequency: 1.032417922775139e-4
allele num: 9686
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66066
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele num: 66102
num of homozygotes: 0

Other
type: Population
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Latino
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African
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South Asian
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FS
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DP
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele num: 66242
num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 1.0e-4

FS
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SIO_000300: 5.994e0

ClippingRankSum
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SIO_000300: -9.3e-2

VQSLOD
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.688858e6

ReadPosRankSum
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SIO_000300: 3.11e-1

MQRankSum
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SIO_000300: 9.01e-1

QD
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SIO_000300: 1.337e1

BaseQRankSum
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SIO_000300: -1.355e0

GenotypeDepth
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 18

GenotypeQuality
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bin: 2.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 18
allele frequency: 2.711006687149828e-4
allele num: 66396
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.063e0

ClippingRankSum
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SIO_000300: 2.28e-1

MQ
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SIO_000300: 5.966e1

InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.02e-1

QD
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SIO_000300: 1.179e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 94
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506114826194349e-5
allele num: 66396
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.02e-1

BaseQRankSum
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SIO_000300: -3.063e0

VQSLOD
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InbreedingCoeff
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SIO_000300: 4.0e-4

MQ
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SIO_000300: 5.966e1

ReadPosRankSum
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MQRankSum
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SIO_000300: -5.0e-2

QD
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SIO_000300: 1.179e1

ClippingRankSum
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SIO_000300: 2.28e-1

DP
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SIO_000300: 1.693672e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 345
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.271e1

FS
type: SiteQuality
SIO_000300: 1.501e0

ReadPosRankSum
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SIO_000300: -6.8e-1

DP
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SIO_000300: 1.696076e6

MQRankSum
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SIO_000300: 5.93e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -7.9e-2

InbreedingCoeff
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SIO_000300: 2.0e-4

ClippingRankSum
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SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 77

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

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

South Asian
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allele count: 77
allele frequency: 4.676302684319203e-3
allele num: 16466
num of homozygotes: 0

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

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

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8622
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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 (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele num: 9738
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Other
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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FS
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.004085556356645e-5
allele num: 66576
num of homozygotes: 0

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

VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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MQRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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South Asian
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African
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European (Non-Finnish)
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QD
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BaseQRankSum
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MQ
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FS
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
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num of homozygotes: 0

Other
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African
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South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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FS
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VQSLOD
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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SIO_000300: -8.4e-1

InbreedingCoeff
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SIO_000300: 1.98e-2

GenotypeDepth
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variant carriers: 2

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

European (Finnish)
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allele count: 6
allele frequency: 9.079903147699758e-4
allele num: 6608
num of homozygotes: 0

Latino
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African
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66628
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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QD
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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QD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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Other
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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allele num: 9748
num of homozygotes: 0

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

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

African
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East Asian
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European (Non-Finnish)
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allele num: 66612
num of homozygotes: 0

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

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

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

Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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allele num: 66530
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East Asian
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South Asian
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InbreedingCoeff
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FS
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QD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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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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Latino
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East Asian
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South Asian
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African
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Other
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MQ
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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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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bin: 6.75e1
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.583330694448843e-5
allele num: 63158
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.563862e6

ReadPosRankSum
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SIO_000300: -5.649999999999999e-1

BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: 4.6e-1

MQRankSum
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SIO_000300: -7.9e-1

InbreedingCoeff
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SIO_000300: 1.4e-3

MQ
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SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.166661388897685e-5
allele num: 63158
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11180
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
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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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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
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SIO_000300: -7.9e-1

BaseQRankSum
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SIO_000300: -2.71e0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11068
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.268230818008878e-4
allele num: 15770
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62240
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.502847e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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SIO_000300: -6.222e-1

QD
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SIO_000300: 1.576e1

ClippingRankSum
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SIO_000300: 6.47e-1

FS
type: SiteQuality
SIO_000300: 8.586e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 37

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

GenotypeQuality
all individuals: 4991
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.191540653079115e-4
allele num: 9126
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.62515860068878e-4
allele num: 11034
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.270325203252033e-4
allele num: 15744
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.146788990825688e-3
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
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allele count: 29
allele frequency: 4.674705009994197e-4
allele num: 62036
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.5e-3

DP
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QD
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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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SIO_000300: 3.02e-1

FS
type: SiteQuality
SIO_000300: 9.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7896
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.617494824016563e-5
allele num: 61824
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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6428
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

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

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

East Asian
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allele count: 2
allele frequency: 2.594706798131811e-4
allele num: 7708
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.153972964061985e-4
allele num: 60660
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

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

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

European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 59742
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Other
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.171312874401794e-4
allele num: 59762
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 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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Latino
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allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

DP
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SIO_000300: 1.296266e6

BaseQRankSum
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SIO_000300: 3.25e0

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -2.2e-3

QD
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SIO_000300: 1.626e1

MQRankSum
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SIO_000300: -2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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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: 10678
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58866
num of homozygotes: 0

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

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

South Asian
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Other
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allele frequency: 0.0e0
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African
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: 6.08e-1

DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58436
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

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

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

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

Other
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num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 15254
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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FS
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QD
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MQRankSum
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SIO_000300: 9.29e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: -4.0e-3

ReadPosRankSum
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SIO_000300: 2.12e-1

DP
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SIO_000300: 1.234727e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.800309653260361e-5
allele num: 55546
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6940
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
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InbreedingCoeff
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MQRankSum
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DP
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FS
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: -2.44e-1

ClippingRankSum
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SIO_000300: 1.35e-1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54790
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele count: 0
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South Asian
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African
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allele frequency: 1.200768491834774e-4
allele num: 8328
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European (Finnish)
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allele count: 0
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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