7-86824202-CATTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824202
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824198
    reference: chr 7
allele count: 3
allele frequency: 2.634120642725437e-5
allele num: 113890
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1909+60_1909+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1579+60_*1579+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1963+60_1963+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*846+60_*846+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1526+60_*1526+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1400+60_1400+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2173+60_2173+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.935_938delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1109+60_*1109+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2173+60_2173+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1526+60_*1526+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1526+60_*1526+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463239
  ensembl transcript: ENST00000582204
  gene symbol: DMTF1
  hgvsc: ENST00000582204.1:c.*45_*48delATTT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1375+60_1375+63delTTTA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-143_432-140delTTTA
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: CATTT
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-86824203-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824203
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824202
    reference: chr 7
allele count: 1
allele frequency: 8.763320246775098e-6
allele num: 114112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1909+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1375+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1579+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.937delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2173+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1526+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463239
  ensembl transcript: ENST00000582204
  gene symbol: DMTF1
  hgvsc: ENST00000582204.1:c.*48delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1109+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*846+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1526+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1400+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-141delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2173+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1963+62delT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1526+62delT
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11362
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: AT
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

7-86824204-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824204
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824204
    reference: chr 7
allele count: 1
allele frequency: 8.80467704444601e-6
allele num: 113576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1526+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1909+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1963+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-143T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2173+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1526+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1375+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463239
  ensembl transcript: ENST00000582204
  gene symbol: DMTF1
  hgvsc: ENST00000582204.1:c.*46T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1109+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*846+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2173+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.935T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1579+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1526+60T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1400+60T>G
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

7-86824204-TTTAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824204
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824200
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 113576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-138_432-135delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2173+65_2173+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1109+65_*1109+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463239
  ensembl transcript: ENST00000582204
  gene symbol: DMTF1
  hgvsc: ENST00000582204.1:c.*46_*50delTTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1909+65_1909+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1526+65_*1526+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1400+65_1400+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.940_943delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*846+65_*846+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1526+65_*1526+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2173+65_2173+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1963+65_1963+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1526+65_*1526+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1375+65_1375+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1579+65_*1579+68delTTAA
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: 3' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: TTTAA
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-86824309-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824309
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824309
    reference: chr 7
allele count: 1
allele frequency: 8.443663874628478e-6
allele num: 118432
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1040A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2174-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1110-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1376-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2174-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1527-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1527-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1910-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1580-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*847-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1527-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1401-38A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1964-38A>C
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-86824312-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824312
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824312
    reference: chr 7
allele count: 2
allele frequency: 1.687906152417926e-5
allele num: 118490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1401-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2174-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1527-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*847-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1910-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1110-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1527-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1527-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1043A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2174-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1376-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1964-35A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1580-35A>G
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

7-86824313-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824313
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824313
    reference: chr 7
allele count: 5
allele frequency: 4.221047832914043e-5
allele num: 118454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*847-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1527-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1044T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1527-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1110-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1580-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2174-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1527-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1401-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2174-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1376-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1964-34T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1910-34T>C
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

7-86824333-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824333
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824333
    reference: chr 7
allele count: 1
allele frequency: 8.354498061756449e-6
allele num: 119696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1527-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1527-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2174-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1527-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1401-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*847-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1376-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1580-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2174-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1064G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1964-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1110-14G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1910-14G>A
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

7-86824343-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824343
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824343
    reference: chr 7
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1110-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1910-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1527-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1074A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1376-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1527-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2174-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1964-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1527-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.432-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*847-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1580-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1401-4A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2174-4A>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2174-4A>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

7-86824356-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824356
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824356
    reference: chr 7
allele count: 2
allele frequency: 1.657302905251993e-5
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1919T>G
  hgvsp: ENSP00000412532.2:p.Leu640Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.441T>G
  hgvsp: ENSP00000410288.2:p.Ser148Ala
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1385T>G
  hgvsp: ENSP00000415910.2:p.Leu462Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1589T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1087T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1973T>G
  hgvsp: ENSP00000402627.2:p.Leu658Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2183T>G
  hgvsp: ENSP00000378193.5:p.Leu728Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1410T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1536T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2183T>G
  hgvsp: ENSP00000332171.7:p.Leu728Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1536T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1536T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*856T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1119T>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10969
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu728Arg
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: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-86824360-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824360
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824360
    reference: chr 7
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1389A>G
  hgvsp: ENST00000414194.2:c.1389A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1540A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1540A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1977A>G
  hgvsp: ENST00000413276.2:c.1977A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1091A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*860A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1123A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.445A>G
  hgvsp: ENSP00000410288.2:p.Asn149Ser
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1540A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1923A>G
  hgvsp: ENST00000432937.2:c.1923A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2187A>G
  hgvsp: ENST00000331242.7:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1414A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1593A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2187A>G
  hgvsp: ENST00000394703.5:c.2187A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn149Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

7-86824364-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824364
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824364
    reference: chr 7
allele count: 1
allele frequency: 8.276227364518158e-6
allele num: 120828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*864C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.449C>G
  hgvsp: ENSP00000410288.2:p.Ile150Met
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1927C>G
  hgvsp: ENSP00000412532.2:p.His643Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1597C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1544C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.1981C>G
  hgvsp: ENSP00000402627.2:p.His661Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1095C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2191C>G
  hgvsp: ENSP00000332171.7:p.His731Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1418C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1393C>G
  hgvsp: ENSP00000415910.2:p.His465Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2191C>G
  hgvsp: ENSP00000378193.5:p.His731Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1544C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1544C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1127C>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His731Asp
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/7-86824385-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824385
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824385
    reference: chr 7
allele count: 5
allele frequency: 4.13352953820208e-5
allele num: 120962
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2212A>C
  hgvsp: ENSP00000378193.5:p.Ile738Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.470A>C
  hgvsp: ENST00000454008.2:c.470A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1565A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1565A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2212A>C
  hgvsp: ENSP00000332171.7:p.Ile738Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1618A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2002A>C
  hgvsp: ENSP00000402627.2:p.Ile668Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1414A>C
  hgvsp: ENSP00000415910.2:p.Ile472Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1948A>C
  hgvsp: ENSP00000412532.2:p.Ile650Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1148A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*885A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1116A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1439A>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1565A>C
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile738Leu
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: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

7-86824396-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824396
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824396
    reference: chr 7
allele count: 2
allele frequency: 1.653521173338625e-5
allele num: 120954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*896C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2013C>T
  hgvsp: ENST00000413276.2:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1127C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1425C>T
  hgvsp: ENST00000414194.2:c.1425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1576C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1959C>T
  hgvsp: ENST00000432937.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.481C>T
  hgvsp: ENSP00000410288.2:p.Pro161Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2223C>T
  hgvsp: ENST00000331242.7:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2223C>T
  hgvsp: ENST00000394703.5:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1576C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1450C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1629C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1576C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1159C>T
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro161Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

7-86824401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824401
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824401
    reference: chr 7
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1164G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.486G>A
  hgvsp: ENSP00000410288.2:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1581G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1634G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1581G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2018G>A
  hgvsp: ENSP00000402627.2:p.Gly673Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1964G>A
  hgvsp: ENSP00000412532.2:p.Gly655Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1581G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2228G>A
  hgvsp: ENSP00000332171.7:p.Gly743Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1430G>A
  hgvsp: ENSP00000415910.2:p.Gly477Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*901G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1132G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1455G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2228G>A
  hgvsp: ENSP00000378193.5:p.Gly743Asp
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly743Asp
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

7-86824402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824402
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824402
    reference: chr 7
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1965C>T
  hgvsp: ENST00000432937.2:c.1965C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1165C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1635C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2019C>T
  hgvsp: ENST00000413276.2:c.2019C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1582C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1456C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2229C>T
  hgvsp: ENST00000331242.7:c.2229C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2229C>T
  hgvsp: ENST00000394703.5:c.2229C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1431C>T
  hgvsp: ENST00000414194.2:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1133C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1582C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.487C>T
  hgvsp: ENSP00000410288.2:p.Ala163Val
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*902C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1582C>T
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala163Val
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

7-86824404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824404
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824404
    reference: chr 7
allele count: 8
allele frequency: 6.614522183453773e-5
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1167G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1135G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2021G>A
  hgvsp: ENSP00000402627.2:p.Ser674Asn
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2231G>A
  hgvsp: ENSP00000332171.7:p.Ser744Asn
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1584G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.489G>A
  hgvsp: ENSP00000410288.2:p.Val164Ile
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2231G>A
  hgvsp: ENSP00000378193.5:p.Ser744Asn
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*904G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1637G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1433G>A
  hgvsp: ENSP00000415910.2:p.Ser478Asn
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1458G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1967G>A
  hgvsp: ENSP00000412532.2:p.Ser656Asn
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1584G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1584G>A
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14901
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser744Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

7-86824405-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824405
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824405
    reference: chr 7
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1459T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1434T>A
  hgvsp: ENSP00000415910.2:p.Ser478Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1638T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2232T>A
  hgvsp: ENSP00000332171.7:p.Ser744Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1585T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1585T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1168T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2022T>A
  hgvsp: ENSP00000402627.2:p.Ser674Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2232T>A
  hgvsp: ENSP00000378193.5:p.Ser744Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.490T>A
  hgvsp: ENSP00000410288.2:p.Val164Asp
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1968T>A
  hgvsp: ENSP00000412532.2:p.Ser656Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*905T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1136T>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1585T>A
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser744Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

7-86824406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824406
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824406
    reference: chr 7
allele count: 2
allele frequency: 1.653685237551884e-5
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1435C>T
  hgvsp: ENSP00000415910.2:p.Pro479Ser
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1169C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2023C>T
  hgvsp: ENSP00000402627.2:p.Pro675Ser
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1460C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2233C>T
  hgvsp: ENSP00000332171.7:p.Pro745Ser
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1639C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*906C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2233C>T
  hgvsp: ENSP00000378193.5:p.Pro745Ser
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1137C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1586C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.491C>T
  hgvsp: ENST00000454008.2:c.491C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1586C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1586C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1969C>T
  hgvsp: ENSP00000412532.2:p.Pro657Ser
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro745Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-86824408-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824408
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824408
    reference: chr 7
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1171T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1462T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1971T>C
  hgvsp: ENST00000432937.2:c.1971T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1139T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2235T>C
  hgvsp: ENST00000331242.7:c.2235T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1588T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1588T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1588T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.493T>C
  hgvsp: ENSP00000410288.2:p.Leu165Pro
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1641T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1437T>C
  hgvsp: ENST00000414194.2:c.1437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2235T>C
  hgvsp: ENST00000394703.5:c.2235T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2025T>C
  hgvsp: ENST00000413276.2:c.2025T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*908T>C
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu165Pro
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: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

7-86824422-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824422
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824422
    reference: chr 7
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1602C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*922C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1451C>G
  hgvsp: ENSP00000415910.2:p.Ser484Ter
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2039C>G
  hgvsp: ENSP00000402627.2:p.Ser680Ter
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1602C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1185C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1655C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1602C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2249C>G
  hgvsp: ENSP00000332171.7:p.Ser750Ter
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1476C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1985C>G
  hgvsp: ENSP00000412532.2:p.Ser662Ter
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2249C>G
  hgvsp: ENSP00000378193.5:p.Ser750Ter
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1153C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.507C>G
  hgvsp: ENSP00000410288.2:p.Gln170Glu
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser750Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

7-86824429-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824429
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824429
    reference: chr 7
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2046T>G
  hgvsp: ENSP00000402627.2:p.Asp682Glu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2256T>G
  hgvsp: ENSP00000332171.7:p.Asp752Glu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1662T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1609T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1160T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1609T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.514T>G
  hgvsp: ENSP00000410288.2:p.Met172Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2256T>G
  hgvsp: ENSP00000378193.5:p.Asp752Glu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1192T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1458T>G
  hgvsp: ENSP00000415910.2:p.Asp486Glu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1609T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1992T>G
  hgvsp: ENSP00000412532.2:p.Asp664Glu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1483T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*929T>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp752Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

7-86824432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824432
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824432
    reference: chr 7
allele count: 5
allele frequency: 4.141884391722858e-5
allele num: 120718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.1995C>T
  hgvsp: ENST00000432937.2:c.1995C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2049C>T
  hgvsp: ENST00000413276.2:c.2049C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1612C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1486C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2259C>T
  hgvsp: ENST00000394703.5:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*932C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1195C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2259C>T
  hgvsp: ENST00000331242.7:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.517C>T
  hgvsp: ENSP00000410288.2:p.Ser173Leu
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1163C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1461C>T
  hgvsp: ENST00000414194.2:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1612C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1665C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1612C>T
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser173Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

7-86824444-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824444
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824444
    reference: chr 7
allele count: 5
allele frequency: 4.149653089001759e-5
allele num: 120492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1498A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1624A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1473A>G
  hgvsp: ENST00000414194.2:c.1473A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*944A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.2007A>G
  hgvsp: ENST00000432937.2:c.2007A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1175A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1677A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2061A>G
  hgvsp: ENST00000413276.2:c.2061A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2271A>G
  hgvsp: ENST00000331242.7:c.2271A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1207A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.529A>G
  hgvsp: ENST00000454008.2:c.529A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2271A>G
  hgvsp: ENST00000394703.5:c.2271A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1624A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1624A>G
  variant of: http://identifiers.org/hgnc/14603
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter177Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

7-86824447-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824447
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824447
    reference: chr 7
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2064C>G
  hgvsp: ENSP00000402627.2:p.Asn688Lys
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*2C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1501C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1627C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.2010C>G
  hgvsp: ENSP00000412532.2:p.Asn670Lys
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1476C>G
  hgvsp: ENSP00000415910.2:p.Asn492Lys
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*947C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1178C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2274C>G
  hgvsp: ENSP00000378193.5:p.Asn758Lys
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1627C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2274C>G
  hgvsp: ENSP00000332171.7:p.Asn758Lys
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1680C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1627C>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1210C>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn758Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

7-86824447-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824447
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824445
    reference: chr 7
allele count: 2
allele frequency: 1.661074382910867e-5
allele num: 120404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1478_1479delGT
  hgvsp: ENSP00000415910.2:p.Cys493SerfsTer4
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1682_*1683delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1180_1181delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2276_2277delGT
  hgvsp: ENSP00000378193.5:p.Cys759SerfsTer4
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1503_1504delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*4_*5delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1629_*1630delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2276_2277delGT
  hgvsp: ENSP00000332171.7:p.Cys759SerfsTer4
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2066_2067delGT
  hgvsp: ENSP00000402627.2:p.Cys689SerfsTer4
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.2012_2013delGT
  hgvsp: ENSP00000412532.2:p.Cys671SerfsTer4
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1629_*1630delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*949_*950delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1629_*1630delGT
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1212_*1213delGT
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10992
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys759SerfsTer4
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: CTG
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-86824448-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824448
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824448
    reference: chr 7
allele count: 2
allele frequency: 1.661488361274029e-5
allele num: 120374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*3T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1628T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.2065T>C
  hgvsp: ENSP00000402627.2:p.Cys689Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1681T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.1477T>C
  hgvsp: ENSP00000415910.2:p.Cys493Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.2275T>C
  hgvsp: ENSP00000378193.5:p.Cys759Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.2011T>C
  hgvsp: ENSP00000412532.2:p.Cys671Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*948T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1502T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1179T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.2275T>C
  hgvsp: ENSP00000332171.7:p.Cys759Arg
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1211T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1628T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1628T>C
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys759Arg
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: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

7-86824458-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824458
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824458
    reference: chr 7
allele count: 1
allele frequency: 8.342510094437214e-6
allele num: 119868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1691A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*2A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*2A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*13A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1189A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1221A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1638A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*2A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*958A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1638A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.*2A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*2A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1512A>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1638A>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

7-86824462-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824462
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824462
    reference: chr 7
allele count: 1
allele frequency: 8.364141253617491e-6
allele num: 119558
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*6T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.*6T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*962T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1516T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*6T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1642T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*6T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1695T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*17T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1642T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1642T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*6T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1193T>G
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1225T>G
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

7-86824472-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824472
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824472
    reference: chr 7
allele count: 1
allele frequency: 8.419209267865562e-6
allele num: 118776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1235T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1652T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*16T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*16T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1526T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1652T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*16T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1652T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*16T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1203T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.*16T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*27T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*972T>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1705T>C
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10445
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-86824474-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824474
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824474
    reference: chr 7
allele count: 18
allele frequency: 1.519474599449613e-4
allele num: 118462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1654G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*18G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*18G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*974G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1707G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1654G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1654G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1205G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1237G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*18G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000412532
  ensembl transcript: ENST00000432937
  gene symbol: DMTF1
  hgvsc: ENST00000432937.2:c.*18G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*29G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*18G>C
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1528G>C
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24048
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

7-86824488-AGAAGGCACACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824488
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824477
    reference: chr 7
allele count: 1
allele frequency: 8.511797351128664e-6
allele num: 117484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7820
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: AGAAGGCACACT
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS

7-86824500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824500
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824500
    reference: chr 7
allele count: 2
allele frequency: 1.72824997407625e-5
allele num: 115724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*44G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1263G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*44G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1680G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*44G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1680G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1231G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1680G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1554G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*1000G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*44G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1733G>A
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*55G>A
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

7-86824508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86824508
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86824508
    reference: chr 7
allele count: 3001
allele frequency: 2.673591932006486e-2
allele num: 112246
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000378193
  ensembl transcript: ENST00000394703
  gene symbol: DMTF1
  hgvsc: ENST00000394703.5:c.*52C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000410288
  ensembl transcript: ENST00000454008
  gene symbol: DMTF1
  hgvsc: ENST00000454008.2:c.*63C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000411908
  ensembl transcript: ENST00000425406
  gene symbol: DMTF1
  hgvsc: ENST00000425406.1:c.*1741C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000463638
  ensembl transcript: ENST00000579850
  gene symbol: DMTF1
  hgvsc: ENST00000579850.1:c.*1008C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000464596
  ensembl transcript: ENST00000579677
  gene symbol: DMTF1
  hgvsc: ENST00000579677.1:c.*1688C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000402627
  ensembl transcript: ENST00000413276
  gene symbol: DMTF1
  hgvsc: ENST00000413276.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000407941
  ensembl transcript: ENST00000412139
  gene symbol: DMTF1
  hgvsc: ENST00000412139.2:c.*1688C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000415910
  ensembl transcript: ENST00000414194
  gene symbol: DMTF1
  hgvsc: ENST00000414194.2:c.*52C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000488352
  gene symbol: DMTF1
  hgvsc: ENST00000488352.2:n.1562C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000332171
  ensembl transcript: ENST00000331242
  gene symbol: DMTF1
  hgvsc: ENST00000331242.7:c.*52C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135164
  ensembl transcript: ENST00000580010
  gene symbol: DMTF1
  hgvsc: ENST00000580010.1:n.1239C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000448775
  ensembl transcript: ENST00000547146
  gene symbol: DMTF1
  hgvsc: ENST00000547146.2:c.*1271C>T
  variant of: http://identifiers.org/hgnc/14603
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135164
  ensembl protein: ENSP00000389774
  ensembl transcript: ENST00000447863
  gene symbol: DMTF1
  hgvsc: ENST00000447863.1:c.*1688C>T
  variant of: http://identifiers.org/hgnc/14603
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 13651
  bin: 1.75e1
  variant carriers: 723
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.5e0
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 1.25e1
  variant carriers: 399
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 2.75e1
  variant carriers: 505
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 4.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
num of homozygotes: 44
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

7-86825902-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825902
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825902
    reference: chr 7
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*50G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8716
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10370
  num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

7-86825907-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825907
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825907
    reference: chr 7
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*45A>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*45A>G
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45432
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 906
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-86825922-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825922
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825922
    reference: chr 7
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*30T>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.491T>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*30T>G
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-86825928-G-GGTAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825928
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825932
    reference: chr 7
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: GGTAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.481_484dupTTAC
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*20_*23dupTTAC
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*20_*23dupTTAC
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

7-86825930-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825930
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825931
    reference: chr 7
allele count: 43
allele frequency: 3.555482057218456e-4
allele num: 120940
alternate allele: TA
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*21dupT
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*21dupT
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.482dupT
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31539
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8710
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

7-86825938-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825938
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825935
    reference: chr 7
allele count: 6
allele frequency: 4.960399477504589e-5
allele num: 120958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.472_474delGAG
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*11_*13delGAG
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*11_*13delGAG
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8716
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: TCTC
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

7-86825945-G-GGCAGCCTCACCTTCCCACATCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825945
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825967
    reference: chr 7
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: GGCAGCCTCACCTTCCCACATCA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45880
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

7-86825949-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825949
    reference: chr 7
allele count: 2
allele frequency: 1.653329806229747e-5
allele num: 120968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*3C>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.464C>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*3C>G
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8726
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-86825950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825950
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825950
    reference: chr 7
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.*2G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.463G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.*2G>A
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8726
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45887
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

7-86825953-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825953
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825953
    reference: chr 7
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.356G>C
  hgvsp: ENSP00000257637.3:p.Ter119SerextTer19
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.356G>C
  hgvsp: ENSP00000398083.1:p.Ter119SerextTer19
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.460G>C
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45888
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ter119SerextTer19
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-86825956-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825956
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825956
    reference: chr 7
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.353G>C
  hgvsp: ENSP00000257637.3:p.Arg118Thr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.457G>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.353G>C
  hgvsp: ENSP00000398083.1:p.Arg118Thr
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg118Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-86825958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825958
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825958
    reference: chr 7
allele count: 1
allele frequency: 8.267332462507647e-6
allele num: 120958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.351A>G
  hgvsp: ENST00000257637.3:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.351A>G
  hgvsp: ENST00000433078.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.455A>G
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45909
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly117Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

7-86825960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825960
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825960
    reference: chr 7
allele count: 2
allele frequency: 1.653439153439154e-5
allele num: 120960
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.349G>A
  hgvsp: ENSP00000398083.1:p.Gly117Arg
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.349G>A
  hgvsp: ENSP00000257637.3:p.Gly117Arg
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.453G>A
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45907
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly117Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

7-86825962-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825962
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825962
    reference: chr 7
allele count: 2
allele frequency: 1.653411815280832e-5
allele num: 120962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.347T>A
  hgvsp: ENSP00000257637.3:p.Val116Glu
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.347T>A
  hgvsp: ENSP00000398083.1:p.Val116Glu
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.451T>A
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45902
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val116Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum

7-86825969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825969
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825969
    reference: chr 7
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.340C>T
  hgvsp: ENSP00000257637.3:p.His114Tyr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.340C>T
  hgvsp: ENSP00000398083.1:p.His114Tyr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.444C>T
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8712
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45869
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His114Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

7-86825977-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825977
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825977
    reference: chr 7
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.436T>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.332T>C
  hgvsp: ENSP00000257637.3:p.Leu111Pro
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.332T>C
  hgvsp: ENSP00000398083.1:p.Leu111Pro
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8701
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45841
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu111Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-86825980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825980
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825980
    reference: chr 7
allele count: 15
allele frequency: 1.241331369271256e-4
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.329A>G
  hgvsp: ENSP00000257637.3:p.Asn110Ser
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.433A>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.329A>G
  hgvsp: ENSP00000398083.1:p.Asn110Ser
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14028
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn110Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS

7-86825984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825984
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825984
    reference: chr 7
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.325G>A
  hgvsp: ENSP00000257637.3:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.429G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.325G>A
  hgvsp: ENSP00000398083.1:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala109Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-86825988-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825988
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825988
    reference: chr 7
allele count: 3
allele frequency: 2.483978339708878e-5
allele num: 120774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.425A>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.321A>C
  hgvsp: ENST00000257637.3:c.321A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.321A>C
  hgvsp: ENST00000433078.1:c.321A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 45826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 8676
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ile107Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

7-86825989-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825989
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825989
    reference: chr 7
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.424T>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.320T>C
  hgvsp: ENSP00000398083.1:p.Ile107Thr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.320T>C
  hgvsp: ENSP00000257637.3:p.Ile107Thr
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8675
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile107Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

7-86825990-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825990
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825990
    reference: chr 7
allele count: 3
allele frequency: 2.484307457890989e-5
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.423A>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.319A>G
  hgvsp: ENSP00000257637.3:p.Ile107Val
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.319A>G
  hgvsp: ENSP00000398083.1:p.Ile107Val
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45790
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile107Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

7-86825993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825993
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825993
    reference: chr 7
allele count: 2
allele frequency: 1.656781205474005e-5
allele num: 120716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.316T>C
  hgvsp: ENSP00000257637.3:p.Cys106Arg
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.420T>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.316T>C
  hgvsp: ENSP00000398083.1:p.Cys106Arg
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 8662
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genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
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genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys106Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-86825994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825994
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825994
    reference: chr 7
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.315G>A
  hgvsp: ENST00000257637.3:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.419G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.315G>A
  hgvsp: ENST00000433078.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45727
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 202
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 8657
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu105Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

7-86825997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86825997
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86825997
    reference: chr 7
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.312G>A
  hgvsp: ENSP00000398083.1:p.Met104Ile
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.416G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.312G>A
  hgvsp: ENSP00000257637.3:p.Met104Ile
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Met104Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

7-86826013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826013
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826013
    reference: chr 7
allele count: 3
allele frequency: 2.493019545273235e-5
allele num: 120336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.400T>C
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.296T>C
  hgvsp: ENSP00000398083.1:p.Ile99Thr
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.296T>C
  hgvsp: ENSP00000257637.3:p.Ile99Thr
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
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genotype depth: GenotypeDepth
  all individuals: 376
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 197
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile99Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

7-86826014-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826014
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826014
    reference: chr 7
allele count: 3
allele frequency: 2.493185293531015e-5
allele num: 120328
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.295A>G
  hgvsp: ENSP00000398083.1:p.Ile99Val
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.399A>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.295A>G
  hgvsp: ENSP00000257637.3:p.Ile99Val
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 13813
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
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genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 649
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ile99Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

7-86826019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826019
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826019
    reference: chr 7
allele count: 2
allele frequency: 1.664447403462051e-5
allele num: 120160
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.290A>G
  hgvsp: ENSP00000398083.1:p.Tyr97Cys
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.290A>G
  hgvsp: ENSP00000257637.3:p.Tyr97Cys
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.394A>G
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13691
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 1
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  variant carriers: 0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr97Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

7-86826020-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826020
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826020
    reference: chr 7
allele count: 3
allele frequency: 2.496338703235255e-5
allele num: 120176
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.289T>C
  hgvsp: ENSP00000398083.1:p.Tyr97His
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.289T>C
  hgvsp: ENSP00000257637.3:p.Tyr97His
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.393T>C
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8442
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr97His
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

7-86826021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826021
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826021
    reference: chr 7
allele count: 1
allele frequency: 8.326256015719971e-6
allele num: 120102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.392C>T
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.288C>T
  hgvsp: ENST00000433078.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.288C>T
  hgvsp: ENST00000257637.3:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8424
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr96Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-86826032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826032
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826032
    reference: chr 7
allele count: 1
allele frequency: 8.370021929457456e-6
allele num: 119474
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.277A>G
  hgvsp: ENSP00000398083.1:p.Lys93Glu
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.381A>G
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.277A>G
  hgvsp: ENSP00000257637.3:p.Lys93Glu
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8225
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 22
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genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 190
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genotype quality: GenotypeQuality
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys93Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

7-86826042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826042
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826042
    reference: chr 7
allele count: 4
allele frequency: 3.362757461118117e-5
allele num: 118950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.371G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.267G>A
  hgvsp: ENST00000433078.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.267G>A
  hgvsp: ENST00000257637.3:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13123
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8068
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 573
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genotype quality: GenotypeQuality
  all individuals: 44066
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro89Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

7-86826043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826043
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826043
    reference: chr 7
allele count: 2
allele frequency: 1.683020011107932e-5
allele num: 118834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.370C>T
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.266C>T
  hgvsp: ENSP00000398083.1:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.266C>T
  hgvsp: ENSP00000257637.3:p.Pro89Leu
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44073
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro89Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-86826049-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826049
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826049
    reference: chr 7
allele count: 1
allele frequency: 8.447372867038351e-6
allele num: 118380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.260T>C
  hgvsp: ENSP00000257637.3:p.Leu87Ser
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.260T>C
  hgvsp: ENSP00000398083.1:p.Leu87Ser
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.364T>C
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
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genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 43796
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genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 7963
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu87Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-86826053-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826053
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826053
    reference: chr 7
allele count: 24
allele frequency: 2.037905033625433e-4
allele num: 117768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.256G>A
  hgvsp: ENSP00000398083.1:p.Asp86Asn
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.256G>A
  hgvsp: ENSP00000257637.3:p.Asp86Asn
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.360G>A
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9910
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29039
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12772
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 271
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 196
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 43002
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7846
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Asp86Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

7-86826061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826061
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826061
    reference: chr 7
allele count: 4
allele frequency: 3.437961976140544e-5
allele num: 116348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.248G>A
  hgvsp: ENSP00000257637.3:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.352G>A
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.248G>A
  hgvsp: ENSP00000398083.1:p.Arg83Gln
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28138
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 126
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 361
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41580
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 419
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 174
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg83Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-86826067-CAGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826067
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826064
    reference: chr 7
allele count: 2
allele frequency: 1.749842514173725e-5
allele num: 114296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135185
  ensembl transcript: ENST00000481425
  gene symbol: TMEM243
  hgvsc: ENST00000481425.1:n.343_345delACT
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000257637
  ensembl transcript: ENST00000257637
  gene symbol: TMEM243
  hgvsc: ENST00000257637.3:c.239_241delACT
  hgvsp: ENSP00000257637.3:p.Tyr80del
  variant of: http://identifiers.org/hgnc/21707
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.239_241delACT
  hgvsp: ENSP00000398083.1:p.Tyr80del
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11939
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 380
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 39311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr80del
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: CAGT
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/7-86826075-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86826075
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 86826075
    reference: chr 7
allele count: 4
allele frequency: 3.646308113035551e-5
allele num: 109700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000135185
  ensembl protein: ENSP00000398083
  ensembl transcript: ENST00000433078
  gene symbol: TMEM243
  hgvsc: ENST00000433078.1:c.235-1G>T
  variant of: http://identifiers.org/hgnc/21707
canonical: true
consequence: splice acceptor
filter: PASS
hgvs: c.235-1G>T
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 10162
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 642
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2824
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14737
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11307
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 586
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4739
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2597
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4779
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4486
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.13883047176622e-5
allele num: 63718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.283321194464675e-5
allele num: 13730
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 6.398e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: -1.182e0

DP
type: SiteQuality
SIO_000300: 1.551799e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

QD
type: SiteQuality
SIO_000300: 1.335e1

MQ
type: SiteQuality
SIO_000300: 5.649e1

GenotypeDepth
all individuals: 2822
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4779
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4551
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567005139776858e-5
allele num: 63816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.529e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.547e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.551501e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeDepth
all individuals: 642
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10070
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11510
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2682
bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 841
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 246
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4521
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10257
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variant carriers: 0

GenotypeQuality
all individuals: 4034
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variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4406
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variant carriers: 0

GenotypeQuality
all individuals: 2238
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4871
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variant carriers: 0

GenotypeQuality
all individuals: 705
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4761
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572425938738285e-5
allele num: 63596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

DP
type: SiteQuality
SIO_000300: 1.552165e6

FS
type: SiteQuality
SIO_000300: 2.269e0

QD
type: SiteQuality
SIO_000300: 1.751e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.596e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

GenotypeDepth
all individuals: 441
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1495
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11510
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2823
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14602
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 123
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.596e1

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

DP
type: SiteQuality
SIO_000300: 1.552165e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.751e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

FS
type: SiteQuality
SIO_000300: 2.269e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

GenotypeDepth
all individuals: 1203
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1382
bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 298
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520727516043675e-5
allele num: 65758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15138
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.785e1

FS
type: SiteQuality
SIO_000300: 1.4615e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.682e-1

DP
type: SiteQuality
SIO_000300: 1.770967e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

MQRankSum
type: SiteQuality
SIO_000300: -1.332e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeDepth
all individuals: 1313
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1191
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
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variant carriers: 0

GenotypeDepth
all individuals: 396
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variant carriers: 1

GenotypeDepth
all individuals: 226
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variant carriers: 0

GenotypeDepth
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.25e1
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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European (Finnish)
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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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Latino
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allele frequency: 8.849557522123894e-5
allele num: 11300
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.520218911523259e-5
allele num: 65780
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 1
allele frequency: 1.525785779676533e-4
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.081430352418889e-5
allele num: 65774
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African
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South Asian
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Other
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East Asian
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Latino
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FS
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ReadPosRankSum
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DP
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
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allele num: 10320
num of homozygotes: 0

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

European (Non-Finnish)
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South Asian
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Latino
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allele num: 11380
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African
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European (Finnish)
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East Asian
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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FS
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
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allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

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

Other
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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: 8638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.84e-1

InbreedingCoeff
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SIO_000300: 0.0e0

QD
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MQ
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FS
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ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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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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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: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8640
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
allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.514051275885907e-5
allele num: 66542
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.946e1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
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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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.006072265977274e-5
allele num: 66532
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 3.02e-1

MQ
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SIO_000300: 5.962e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.828235e6

QD
type: SiteQuality
SIO_000300: 1.223e1

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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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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
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
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.14e-2

FS
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SIO_000300: 3.612e0

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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele 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 (Non-Finnish)
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allele num: 66528
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European (Finnish)
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East Asian
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South Asian
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Other
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele num: 11402
num of homozygotes: 0

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

East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66520
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

African
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allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
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 frequency: 0.0e0
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Other
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele frequency: 8.771929824561403e-5
allele num: 11400
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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Other
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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SIO_000300: 5.907e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504709741490866e-5
allele num: 66458
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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VQSLOD
type: SiteQuality
SIO_000300: -1.51e0

ReadPosRankSum
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MQRankSum
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

FS
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SIO_000300: 1.2208e1

ClippingRankSum
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SIO_000300: -5.23e-1

MQ
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SIO_000300: 5.808e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

European (Non-Finnish)
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allele count: 0
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Latino
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African
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East Asian
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Other
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South Asian
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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DP
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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allele num: 66416
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East Asian
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African
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European (Finnish)
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Latino
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Other
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South Asian
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FS
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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African
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.121449559255632e-5
allele num: 16336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.554e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.818791e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.936483346243222e-4
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.554e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.818791e6

FS
type: SiteQuality
SIO_000300: 5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.812125484666901e-5
allele num: 11348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.298e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.109e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

FS
type: SiteQuality
SIO_000300: 1.1101e1

DP
type: SiteQuality
SIO_000300: 1.81776e6

VQSLOD
type: SiteQuality
SIO_000300: -1.114e0

MQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
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: 1.514050387596899e-5
allele num: 66048
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

VQSLOD
type: SiteQuality
SIO_000300: -3.913e-1

FS
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.688e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

DP
type: SiteQuality
SIO_000300: 1.806539e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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 count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65916
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
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
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

VQSLOD
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SIO_000300: -7.209e-1

DP
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SIO_000300: 1.797088e6

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 1.454e0

QD
type: SiteQuality
SIO_000300: 1.588e1

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: -2.296e0

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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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: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526251526251526e-5
allele num: 65520
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
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VQSLOD
type: SiteQuality
SIO_000300: -2.381e-1

DP
type: SiteQuality
SIO_000300: 1.760965e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 4.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

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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variant carriers: 0

GenotypeQuality
all individuals: 4588
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 308
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.780626780626781e-4
allele num: 11232
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8432
num of homozygotes: 0

African
type: Population
allele count: 16
allele frequency: 1.567705271408975e-3
allele num: 10206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.289e0

FS
type: SiteQuality
SIO_000300: 1.757e0

QD
type: SiteQuality
SIO_000300: 1.22e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.741137e6

GenotypeDepth
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5800
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4561
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2310
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26878
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.203079884504331e-4
allele num: 8312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.961e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 1.627372e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.039e1

QD
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 126
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1313
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 456
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6032
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15277
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
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GenotypeQuality
all individuals: 526
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.5e0
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GenotypeQuality
all individuals: 1746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5962
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5970
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4559
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.126856571089084e-5
allele num: 63962
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.374e1

DP
type: SiteQuality
SIO_000300: 1.512249e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

MQ
type: SiteQuality
SIO_000300: 5.85e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.347e0

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.101e0

GenotypeDepth
all individuals: 176
bin: 8.25e1
variant carriers: 9

GenotypeDepth
all individuals: 251
bin: 7.25e1
variant carriers: 9

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 16

GenotypeDepth
all individuals: 13944
bin: 2.25e1
variant carriers: 676

GenotypeDepth
all individuals: 128
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2938
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5448
bin: 5.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1567
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 739
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 2285
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 805
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1196
bin: 7.25e1
variant carriers: 14

GenotypeQuality
all individuals: 6187
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 5814
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 452
bin: 8.75e1
variant carriers: 22

GenotypeQuality
all individuals: 1148
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 4167
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 438
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5181
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 2980
bin: 6.75e1
variant carriers: 20

GenotypeQuality
all individuals: 3359
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1827
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 642
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 6257
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7180
bin: 9.75e1
variant carriers: 2882

East Asian
type: Population
allele count: 519
allele frequency: 6.717577012684442e-2
allele num: 7726
num of homozygotes: 13

African
type: Population
allele count: 119
allele frequency: 1.23546511627907e-2
allele num: 9632
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1990
allele frequency: 3.210816741424376e-2
allele num: 61978
num of homozygotes: 28

European (Finnish)
type: Population
allele count: 107
allele frequency: 1.667705735660848e-2
allele num: 6416
num of homozygotes: 1

South Asian
type: Population
allele count: 133
allele frequency: 8.929770377333154e-3
allele num: 14894
num of homozygotes: 1

Latino
type: Population
allele count: 119
allele frequency: 1.106770833333333e-2
allele num: 10752
num of homozygotes: 0

Other
type: Population
allele count: 14
allele frequency: 1.650943396226415e-2
allele num: 848
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.17e0

DP
type: SiteQuality
SIO_000300: 1.481458e6

QD
type: SiteQuality
SIO_000300: 1.389e1

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.740647e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.143e0

QD
type: SiteQuality
SIO_000300: 8.34e0

MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.211e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e0

QD
type: SiteQuality
SIO_000300: 1.543e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

FS
type: SiteQuality
SIO_000300: 1.1639e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.031e0

DP
type: SiteQuality
SIO_000300: 1.740573e6

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

DP
type: SiteQuality
SIO_000300: 1.741431e6

FS
type: SiteQuality
SIO_000300: 6.024e0

QD
type: SiteQuality
SIO_000300: 1.276e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.555e0

VQSLOD
type: SiteQuality
SIO_000300: -1.442e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.756567425569177e-5
allele num: 11420
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.268e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.086e0

DP
type: SiteQuality
SIO_000300: 1.741951e6

FS
type: SiteQuality
SIO_000300: 4.522e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.713e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

GenotypeQuality
all individuals: 696
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

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

South Asian
type: Population
allele count: 43
allele frequency: 2.608906686081786e-3
allele num: 16482
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

FS
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.68e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.168e0

DP
type: SiteQuality
SIO_000300: 1.74281e6

MQ
type: SiteQuality
SIO_000300: 6.004e1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.949270326615705e-4
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.826e1

QD
type: SiteQuality
SIO_000300: 1.543e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

DP
type: SiteQuality
SIO_000300: 1.741086e6

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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South Asian
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Latino
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European (Finnish)
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BaseQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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QD
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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ReadPosRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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Other
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FS
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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DP
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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East Asian
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MQRankSum
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MQ
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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South Asian
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Latino
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African
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East Asian
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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East Asian
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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QD
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FS
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ReadPosRankSum
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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African
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Latino
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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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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African
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South Asian
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East Asian
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeQuality
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South Asian
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African
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Latino
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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DP
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FS
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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African
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Latino
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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GenotypeQuality
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.736242e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.320185614849188e-4
allele num: 8620
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.735996e6

QD
type: SiteQuality
SIO_000300: 1.491e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
all individuals: 671
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.053435114503817e-4
allele num: 6550
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 4.376e0

DP
type: SiteQuality
SIO_000300: 1.735117e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.832e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.695e0

DP
type: SiteQuality
SIO_000300: 1.734797e6

MQ
type: SiteQuality
SIO_000300: 5.906e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.162e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
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Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.733963e6

QD
type: SiteQuality
SIO_000300: 6.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.981e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.035e0

FS
type: SiteQuality
SIO_000300: 1.583e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.21e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

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

East Asian
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allele count: 3
allele frequency: 3.492433061699651e-4
allele num: 8590
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.265e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 1.726063e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

FS
type: SiteQuality
SIO_000300: 1.445e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510254628930438e-5
allele num: 66214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
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African
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allele count: 2
allele frequency: 1.932367149758454e-4
allele num: 10350
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.709e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.72e0

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

DP
type: SiteQuality
SIO_000300: 1.725889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51267622678042e-5
allele num: 66108
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.101281269066504e-5
allele num: 16390
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

FS
type: SiteQuality
SIO_000300: 1.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.53e0

MQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
SIO_000300: 1.721113e6

QD
type: SiteQuality
SIO_000300: 1.276e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.651113467656416e-4
allele num: 11316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

FS
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 1.720764e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.573e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513546238837597e-5
allele num: 66070
num of homozygotes: 0

Latino
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.71975e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.756e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
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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: 6514
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65672
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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African
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allele frequency: 9.738994935722633e-5
allele num: 10268
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.522e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.125574272588055e-5
allele num: 65300
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 2.879e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.788566953797964e-5
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East Asian
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11222
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.685405e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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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: 1.540167570231641e-5
allele num: 64928
num of homozygotes: 0

South Asian
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East Asian
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African
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Other
type: Population
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num of homozygotes: 0

MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.394829830760647e-4
allele num: 64524
num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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Latino
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allele count: 13
allele frequency: 1.16571018651363e-3
allele num: 11152
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.895111814763506e-5
allele num: 10106
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.602e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.657999e6

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 4.634e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.223549912870301e-5
allele num: 16068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.033423667570009e-5
allele num: 11070
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.198178768272226e-4
allele num: 8346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001803245842517e-4
allele num: 9982
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

FS
type: SiteQuality
SIO_000300: 4.227e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.623608e6

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

GenotypeQuality
all individuals: 8578
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.214813862277374e-5
allele num: 62212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15876
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 3.023e0

MQRankSum
type: SiteQuality
SIO_000300: -1.318e0

QD
type: SiteQuality
SIO_000300: 1.368e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.728e1

DP
type: SiteQuality
SIO_000300: 1.570132e6