1-55161084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161084
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161084
    reference: chr 1
allele count: 1
allele frequency: 9.595271450229326e-6
allele num: 104218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*465G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2850G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1157G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.358G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*671G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2885G>A
  hgvsp: ENSP00000396622.2:p.Arg962His
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1017G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1017G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1589G>A
  hgvsp: ENSP00000387048.1:p.Arg530His
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2885G>A
  hgvsp: ENSP00000343211.5:p.Arg962His
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2885G>A
  hgvsp: ENSP00000379044.2:p.Arg962His
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1439G>A
  hgvsp: ENSP00000401130.2:p.Arg480His
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1017G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1017G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2885G>A
  hgvsp: ENSP00000410192.2:p.Arg962His
  variant of: http://identifiers.org/hgnc/49180
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36868
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg962His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-55161085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161085
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161085
    reference: chr 1
allele count: 218
allele frequency: 2.075202284626368e-3
allele num: 105050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*466C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1018C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2886C>T
  hgvsp: ENST00000339553.5:c.2886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1018C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1018C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2886C>T
  hgvsp: ENST00000421030.2:c.2886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1018C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2886C>T
  hgvsp: ENST00000414150.2:c.2886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2886C>T
  hgvsp: ENST00000395690.2:c.2886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.359C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1440C>T
  hgvsp: ENST00000454855.2:c.1440C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1590C>T
  hgvsp: ENST00000409996.1:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1158C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2851C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37124
  bin: 2.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
hgvs: p.Arg962Arg
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-55161095-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161095
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161095
    reference: chr 1
allele count: 2
allele frequency: 1.85776919075574e-5
allele num: 107656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.369C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2896C>A
  hgvsp: ENSP00000396622.2:p.Leu966Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1028C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1600C>A
  hgvsp: ENSP00000387048.1:p.Leu534Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1028C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1450C>A
  hgvsp: ENSP00000401130.2:p.Leu484Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2896C>A
  hgvsp: ENSP00000379044.2:p.Leu966Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1028C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1028C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1168C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*682C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*476C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2896C>A
  hgvsp: ENSP00000410192.2:p.Leu966Met
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2896C>A
  hgvsp: ENSP00000343211.5:p.Leu966Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2861C>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu966Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

1-55161096-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161096
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161096
    reference: chr 1
allele count: 1
allele frequency: 9.258573439004518e-6
allele num: 108008
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2897T>C
  hgvsp: ENSP00000396622.2:p.Leu966Pro
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1451T>C
  hgvsp: ENSP00000401130.2:p.Leu484Pro
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2862T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2897T>C
  hgvsp: ENSP00000379044.2:p.Leu966Pro
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1601T>C
  hgvsp: ENSP00000387048.1:p.Leu534Pro
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*477T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1029T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1029T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.370T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2897T>C
  hgvsp: ENSP00000343211.5:p.Leu966Pro
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1029T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*683T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2897T>C
  hgvsp: ENSP00000410192.2:p.Leu966Pro
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1029T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1169T>C
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu966Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

1-55161102-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161102
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161103
    reference: chr 1
allele count: 1
allele frequency: 9.199124243372031e-6
allele num: 108706
alternate allele: TC
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2906dupC
  hgvsp: ENSP00000410192.2:p.Leu970AlafsTer65
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1610dupC
  hgvsp: ENSP00000387048.1:p.Leu538AlafsTer65
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.379dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*486dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2906dupC
  hgvsp: ENSP00000343211.5:p.Leu970AlafsTer32
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1038dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2906dupC
  hgvsp: ENSP00000379044.2:p.Leu970AlafsTer32
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1460dupC
  hgvsp: ENSP00000401130.2:p.Leu488AlafsTer65
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*692dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1178dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1038dupC
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2906dupC
  hgvsp: ENSP00000396622.2:p.Leu970AlafsTer65
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1038dupC
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1038dupC
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2871dupC
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu970AlafsTer65
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-55161104-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161104
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161104
    reference: chr 1
allele count: 1
allele frequency: 9.182736455463728e-6
allele num: 108900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2905C>A
  hgvsp: ENSP00000343211.5:p.Pro969Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1037C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2905C>A
  hgvsp: ENSP00000410192.2:p.Pro969Thr
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*485C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2905C>A
  hgvsp: ENSP00000379044.2:p.Pro969Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*691C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1459C>A
  hgvsp: ENSP00000401130.2:p.Pro487Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2905C>A
  hgvsp: ENSP00000396622.2:p.Pro969Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1037C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1609C>A
  hgvsp: ENSP00000387048.1:p.Pro537Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.378C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1037C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1037C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2870C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1177C>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro969Thr
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-55161105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161105
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161105
    reference: chr 1
allele count: 2
allele frequency: 1.834155646448158e-5
allele num: 109042
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2906C>T
  hgvsp: ENSP00000410192.2:p.Pro969Leu
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2871C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1038C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2906C>T
  hgvsp: ENSP00000343211.5:p.Pro969Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1460C>T
  hgvsp: ENSP00000401130.2:p.Pro487Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2906C>T
  hgvsp: ENSP00000379044.2:p.Pro969Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1038C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*486C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1610C>T
  hgvsp: ENSP00000387048.1:p.Pro537Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.379C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1038C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2906C>T
  hgvsp: ENSP00000396622.2:p.Pro969Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1178C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1038C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*692C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro969Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-55161106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161106
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161106
    reference: chr 1
allele count: 1
allele frequency: 9.159522239319997e-6
allele num: 109176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*487G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2907G>A
  hgvsp: ENST00000339553.5:c.2907G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.380G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*693G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2907G>A
  hgvsp: ENST00000395690.2:c.2907G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1461G>A
  hgvsp: ENST00000454855.2:c.1461G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2872G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2907G>A
  hgvsp: ENST00000414150.2:c.2907G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2907G>A
  hgvsp: ENST00000421030.2:c.2907G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1039G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1611G>A
  hgvsp: ENST00000409996.1:c.1611G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1039G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1039G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1179G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1039G>A
  variant of: http://identifiers.org/hgnc/49180
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro969Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-55161107-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161107
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161107
    reference: chr 1
allele count: 4
allele frequency: 3.655839289304842e-5
allele num: 109414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1180C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2908C>T
  hgvsp: ENSP00000343211.5:p.Leu970Phe
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.381C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1462C>T
  hgvsp: ENSP00000401130.2:p.Leu488Phe
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1612C>T
  hgvsp: ENSP00000387048.1:p.Leu538Phe
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2908C>T
  hgvsp: ENSP00000396622.2:p.Leu970Phe
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*694C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2908C>T
  hgvsp: ENSP00000410192.2:p.Leu970Phe
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1040C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1040C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2873C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2908C>T
  hgvsp: ENSP00000379044.2:p.Leu970Phe
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*488C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1040C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1040C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu970Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

1-55161109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161109
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161109
    reference: chr 1
allele count: 2
allele frequency: 1.825950407186941e-5
allele num: 109532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2910C>T
  hgvsp: ENST00000339553.5:c.2910C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*490C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2910C>T
  hgvsp: ENST00000414150.2:c.2910C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1042C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1042C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1614C>T
  hgvsp: ENST00000409996.1:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1042C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1464C>T
  hgvsp: ENST00000454855.2:c.1464C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1042C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2910C>T
  hgvsp: ENST00000421030.2:c.2910C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2910C>T
  hgvsp: ENST00000395690.2:c.2910C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1182C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.383C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2875C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*696C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu970Leu
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: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

1-55161116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161116
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161116
    reference: chr 1
allele count: 1
allele frequency: 9.1476243619532e-6
allele num: 109318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*703C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1621C>T
  hgvsp: ENSP00000387048.1:p.Arg541Ter
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2917C>T
  hgvsp: ENSP00000379044.2:p.Arg973Ter
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.390C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1049C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1049C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1049C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*497C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2882C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2917C>T
  hgvsp: ENSP00000396622.2:p.Arg973Ter
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1471C>T
  hgvsp: ENSP00000401130.2:p.Arg491Ter
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2917C>T
  hgvsp: ENSP00000410192.2:p.Arg973Ter
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1189C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2917C>T
  hgvsp: ENSP00000343211.5:p.Arg973Ter
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1049C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg973Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

1-55161117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161117
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161117
    reference: chr 1
allele count: 3
allele frequency: 2.74333369911116e-5
allele num: 109356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1190G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1050G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*498G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2918G>A
  hgvsp: ENSP00000396622.2:p.Arg973Gln
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2918G>A
  hgvsp: ENSP00000343211.5:p.Arg973Gln
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1050G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1622G>A
  hgvsp: ENSP00000387048.1:p.Arg541Gln
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1472G>A
  hgvsp: ENSP00000401130.2:p.Arg491Gln
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1050G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2918G>A
  hgvsp: ENSP00000410192.2:p.Arg973Gln
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.391G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2883G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2918G>A
  hgvsp: ENSP00000379044.2:p.Arg973Gln
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*704G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1050G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg973Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

1-55161120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161120
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161120
    reference: chr 1
allele count: 1
allele frequency: 9.146285693379919e-6
allele num: 109334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*501G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2921G>A
  hgvsp: ENSP00000343211.5:p.Gly974Asp
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1625G>A
  hgvsp: ENSP00000387048.1:p.Gly542Asp
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1053G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2921G>A
  hgvsp: ENSP00000410192.2:p.Gly974Asp
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2921G>A
  hgvsp: ENSP00000379044.2:p.Gly974Asp
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1193G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*707G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1475G>A
  hgvsp: ENSP00000401130.2:p.Gly492Asp
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1053G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2886G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1053G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1053G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.394G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2921G>A
  hgvsp: ENSP00000396622.2:p.Gly974Asp
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37720
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly974Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

1-55161121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161121
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161121
    reference: chr 1
allele count: 521
allele frequency: 4.7594686934756e-3
allele num: 109466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1476C>T
  hgvsp: ENST00000454855.2:c.1476C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1626C>T
  hgvsp: ENST00000409996.1:c.1626C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1054C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1054C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.395C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2922C>T
  hgvsp: ENST00000421030.2:c.2922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1054C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1194C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2922C>T
  hgvsp: ENST00000339553.5:c.2922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1054C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2922C>T
  hgvsp: ENST00000395690.2:c.2922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2922C>T
  hgvsp: ENST00000414150.2:c.2922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*708C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*502C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2887C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 1.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 2.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37553
  bin: 2.25e1
  variant carriers: 84
genotype quality: GenotypeQuality
hgvs: p.Gly974Gly
num of homozygotes: 11
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-55161122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161122
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161122
    reference: chr 1
allele count: 2
allele frequency: 1.827485380116959e-5
allele num: 109440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2888G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2923G>A
  hgvsp: ENSP00000410192.2:p.Asp975Asn
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1195G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1055G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.396G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*709G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2923G>A
  hgvsp: ENSP00000396622.2:p.Asp975Asn
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1055G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2923G>A
  hgvsp: ENSP00000379044.2:p.Asp975Asn
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1477G>A
  hgvsp: ENSP00000401130.2:p.Asp493Asn
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2923G>A
  hgvsp: ENSP00000343211.5:p.Asp975Asn
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1055G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1627G>A
  hgvsp: ENSP00000387048.1:p.Asp543Asn
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1055G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*503G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp975Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-55161125-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161125
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161125
    reference: chr 1
allele count: 55
allele frequency: 5.042263334494582e-4
allele num: 109078
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2926G>A
  hgvsp: ENSP00000410192.2:p.Glu976Lys
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2926G>A
  hgvsp: ENSP00000343211.5:p.Glu976Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1058G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1198G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*506G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2926G>A
  hgvsp: ENSP00000396622.2:p.Glu976Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2926G>A
  hgvsp: ENSP00000379044.2:p.Glu976Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.399G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*712G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1480G>A
  hgvsp: ENSP00000401130.2:p.Glu494Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1630G>A
  hgvsp: ENSP00000387048.1:p.Glu544Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1058G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1058G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2891G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1058G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37139
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Glu976Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

1-55161135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161135
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161135
    reference: chr 1
allele count: 1
allele frequency: 9.335499169140573e-6
allele num: 107118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2936G>A
  hgvsp: ENSP00000379044.2:p.Arg979Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1640G>A
  hgvsp: ENSP00000387048.1:p.Arg547Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*722G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2936G>A
  hgvsp: ENSP00000343211.5:p.Arg979Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2936G>A
  hgvsp: ENSP00000396622.2:p.Arg979Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.409G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1490G>A
  hgvsp: ENSP00000401130.2:p.Arg497Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1068G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1068G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1068G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*516G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2936G>A
  hgvsp: ENSP00000410192.2:p.Arg979Lys
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2901G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1068G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1208G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34672
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6675
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg979Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

1-55161140-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161140
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161140
    reference: chr 1
allele count: 1
allele frequency: 9.480290476100188e-6
allele num: 105482
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2941A>T
  hgvsp: ENSP00000396622.2:p.Thr981Ser
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1495A>T
  hgvsp: ENSP00000401130.2:p.Thr499Ser
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*521A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1073A>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*727A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.414A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1213A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1073A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1645A>T
  hgvsp: ENSP00000387048.1:p.Thr549Ser
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2941A>T
  hgvsp: ENSP00000410192.2:p.Thr981Ser
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1073A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2906A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2941A>T
  hgvsp: ENSP00000379044.2:p.Thr981Ser
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2941A>T
  hgvsp: ENSP00000343211.5:p.Thr981Ser
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1073A>T
  variant of: http://identifiers.org/hgnc/49180
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr981Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-55161141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161141
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161141
    reference: chr 1
allele count: 14
allele frequency: 1.334629830883334e-4
allele num: 104898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*522C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1074C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2942C>T
  hgvsp: ENSP00000379044.2:p.Thr981Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.415C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1646C>T
  hgvsp: ENSP00000387048.1:p.Thr549Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1496C>T
  hgvsp: ENSP00000401130.2:p.Thr499Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2942C>T
  hgvsp: ENSP00000343211.5:p.Thr981Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2942C>T
  hgvsp: ENSP00000396622.2:p.Thr981Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1214C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2942C>T
  hgvsp: ENSP00000410192.2:p.Thr981Met
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2907C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1074C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1074C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*728C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1074C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11100
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr981Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

1-55161142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161142
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161142
    reference: chr 1
allele count: 3
allele frequency: 2.861066605630579e-5
allele num: 104856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1075G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2943G>A
  hgvsp: ENST00000339553.5:c.2943G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1075G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*729G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1215G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1075G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1497G>A
  hgvsp: ENST00000454855.2:c.1497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1075G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2943G>A
  hgvsp: ENST00000414150.2:c.2943G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2943G>A
  hgvsp: ENST00000395690.2:c.2943G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2943G>A
  hgvsp: ENST00000421030.2:c.2943G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1647G>A
  hgvsp: ENST00000409996.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*523G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.416G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2908G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr981Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

1-55161145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161145
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161145
    reference: chr 1
allele count: 1
allele frequency: 9.677356920277934e-6
allele num: 103334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2946C>T
  hgvsp: ENST00000395690.2:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*732C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1500C>T
  hgvsp: ENST00000454855.2:c.1500C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2946C>T
  hgvsp: ENST00000339553.5:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.419C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1078C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1078C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2946C>T
  hgvsp: ENST00000421030.2:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1650C>T
  hgvsp: ENST00000409996.1:c.1650C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2911C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1078C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*526C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1078C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2946C>T
  hgvsp: ENST00000414150.2:c.2946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1218C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31034
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala982Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

1-55161148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161148
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161148
    reference: chr 1
allele count: 10
allele frequency: 9.923194474765317e-5
allele num: 100774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2949C>T
  hgvsp: ENST00000395690.2:c.2949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1503C>T
  hgvsp: ENST00000454855.2:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*735C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1081C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1221C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1081C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.422C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1653C>T
  hgvsp: ENST00000409996.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2949C>T
  hgvsp: ENST00000414150.2:c.2949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1081C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2949C>T
  hgvsp: ENST00000339553.5:c.2949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2949C>T
  hgvsp: ENST00000421030.2:c.2949C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2914C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1081C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*529C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7599
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10622
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr983Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

1-55161149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161149
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161149
    reference: chr 1
allele count: 2
allele frequency: 1.987636898491384e-5
allele num: 100622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1504G>A
  hgvsp: ENSP00000401130.2:p.Ala502Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*530G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2950G>A
  hgvsp: ENSP00000410192.2:p.Ala984Thr
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1222G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1082G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2950G>A
  hgvsp: ENSP00000379044.2:p.Ala984Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1082G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1654G>A
  hgvsp: ENSP00000387048.1:p.Ala552Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2950G>A
  hgvsp: ENSP00000343211.5:p.Ala984Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1082G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2915G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2950G>A
  hgvsp: ENSP00000396622.2:p.Ala984Thr
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.423G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1082G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*736G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala984Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

1-55161155-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161155
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161155
    reference: chr 1
allele count: 2
allele frequency: 2.073785280272081e-5
allele num: 96442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1510T>C
  hgvsp: ENSP00000401130.2:p.Phe504Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2956T>C
  hgvsp: ENSP00000410192.2:p.Phe986Leu
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*536T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1228T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1660T>C
  hgvsp: ENSP00000387048.1:p.Phe554Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1088T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2956T>C
  hgvsp: ENSP00000379044.2:p.Phe986Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1088T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2956T>C
  hgvsp: ENSP00000343211.5:p.Phe986Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2956T>C
  hgvsp: ENSP00000396622.2:p.Phe986Leu
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*742T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1088T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1088T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2921T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.429T>C
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25176
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe986Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

1-55161157-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161157
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161157
    reference: chr 1
allele count: 3
allele frequency: 3.150201612903226e-5
allele num: 95232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*538C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1090C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2958C>T
  hgvsp: ENST00000339553.5:c.2958C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*744C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2958C>T
  hgvsp: ENST00000421030.2:c.2958C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.431C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2958C>T
  hgvsp: ENST00000395690.2:c.2958C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1090C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1512C>T
  hgvsp: ENST00000454855.2:c.1512C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2958C>T
  hgvsp: ENST00000414150.2:c.2958C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1230C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1662C>T
  hgvsp: ENST00000409996.1:c.1662C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2923C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1090C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1090C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24286
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe986Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

1-55161158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161158
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161158
    reference: chr 1
allele count: 4
allele frequency: 4.202916824276048e-5
allele num: 95172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1091G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*745G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*539G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1091G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1091G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2959G>A
  hgvsp: ENSP00000396622.2:p.Val987Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2959G>A
  hgvsp: ENSP00000410192.2:p.Val987Met
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1231G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2959G>A
  hgvsp: ENSP00000343211.5:p.Val987Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1091G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1513G>A
  hgvsp: ENSP00000401130.2:p.Val505Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1663G>A
  hgvsp: ENSP00000387048.1:p.Val555Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2959G>A
  hgvsp: ENSP00000379044.2:p.Val987Met
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.432G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2924G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val987Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

1-55161162-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161162
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161161
    reference: chr 1
allele count: 1
allele frequency: 1.090369853454292e-5
allele num: 91712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+1delG
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+1delG
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+1delG
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+1delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2930delG
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.438delG
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: AG
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

1-55161171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161171
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161171
    reference: chr 1
allele count: 2
allele frequency: 2.483854942871336e-5
allele num: 80520
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.445C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+8C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+8C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+8C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+8C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2937C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16521
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2964+8C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

1-55161172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161172
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161172
    reference: chr 1
allele count: 10
allele frequency: 1.243193515502623e-4
allele num: 80438
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+9G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+9G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.446G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2938G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+9G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+9G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+9G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

1-55161175-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161175
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161175
    reference: chr 1
allele count: 1
allele frequency: 1.254044292844423e-5
allele num: 79742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.449G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+12G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+12G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2941G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+12G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+12G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+12G>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18950
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16766
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-55161176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161176
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161176
    reference: chr 1
allele count: 1
allele frequency: 1.271164895510246e-5
allele num: 78668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2942G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.450G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+13G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+13G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+13G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+13G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+13G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-55161180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161180
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161180
    reference: chr 1
allele count: 4
allele frequency: 5.350597929318602e-5
allele num: 74758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.454C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+17C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2946C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+17C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+17C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+17C>T
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

1-55161181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161181
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161181
    reference: chr 1
allele count: 2
allele frequency: 2.70841232869292e-5
allele num: 73844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2947G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+18G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.455G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+18G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+18G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+18G>A
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

1-55161186-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161186
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161186
    reference: chr 1
allele count: 3
allele frequency: 4.328129959315579e-5
allele num: 69314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2952C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+23C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+23C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+23C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.460C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+23C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+23C>G
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-55161191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161191
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161191
    reference: chr 1
allele count: 1
allele frequency: 1.537326282130119e-5
allele num: 65048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.465C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2957C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+28C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+28C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+28C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+28C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+28C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23491
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-55161195-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161195
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161195
    reference: chr 1
allele count: 2
allele frequency: 3.220715643015878e-5
allele num: 62098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+32A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+32A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.469A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+32A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2961A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+32A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+32A>G
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

1-55161203-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161203
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161203
    reference: chr 1
allele count: 1
allele frequency: 1.884090737809933e-5
allele num: 53076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.477C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2969C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+40C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+40C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+40C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+40C>G
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24345
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-55161204-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161204
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161204
    reference: chr 1
allele count: 1
allele frequency: 1.928119697670831e-5
allele num: 51864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+41C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+41C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+41C>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.478C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+41C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2970C>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+41C>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

1-55161204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161204
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161204
    reference: chr 1
allele count: 1
allele frequency: 1.928119697670831e-5
allele num: 51864
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+41C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+41C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+41C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.478C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+41C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2970C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-55161205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161205
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161205
    reference: chr 1
allele count: 4
allele frequency: 7.857311228097745e-5
allele num: 50908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+42G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+42G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.479G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+42G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+42G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2971G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+42G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-55161211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161211
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161211
    reference: chr 1
allele count: 2
allele frequency: 4.610844706750277e-5
allele num: 43376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+48C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.485C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+48C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+48C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+48C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2977C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+48C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

1-55161212-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161212
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161212
    reference: chr 1
allele count: 11
allele frequency: 2.569733214969864e-4
allele num: 42806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2978G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+49G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+49G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.486G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+49G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+49G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+49G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12262
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23980
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

1-55161217-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161217
    reference: chr 1
allele count: 2
allele frequency: 5.120589891955553e-5
allele num: 39058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.491A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+54A>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+54A>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2983A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+54A>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+54A>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+54A>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-55161219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161219
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161219
    reference: chr 1
allele count: 3
allele frequency: 8.314855875831486e-5
allele num: 36080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+56G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+56G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2985G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.493G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+56G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+56G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+56G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9325
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

1-55161220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161220
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 35310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+57T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+57T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.494T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+57T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+57T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+2986T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+57T>C
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21454
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-55161238-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161238
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161238
    reference: chr 1
allele count: 5
allele frequency: 2.087857023551027e-4
allele num: 23948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+75A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3004A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.512A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+75A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+75A>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+75A>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+75A>G
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-55161247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161247
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161247
    reference: chr 1
allele count: 1
allele frequency: 5.036768409388536e-5
allele num: 19854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+84G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3013G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.521G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+84G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+84G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+84G>A
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9785
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-55161250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161250
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161250
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 19618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+87C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.524C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3016C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+87C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+87C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+87C>T
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

1-55161251-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161251
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161251
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 19176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+88T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3017T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.525T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+88T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+88T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+88T>C
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 35126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-55161253-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161253
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161253
    reference: chr 1
allele count: 1
allele frequency: 5.258729490954985e-5
allele num: 19016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3019T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1096+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+90T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+90T>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+90T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.527T>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+90T>C
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

1-55161268-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161268
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161268
    reference: chr 1
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.542C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+105C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+105C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-101C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+105C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3034C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+105C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+105C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

1-55161292-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161292
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161292
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 13974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.566G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+129G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+129G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+129G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-77G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3058G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+129G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+129G>C
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

1-55161303-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161303
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161303
    reference: chr 1
allele count: 3
allele frequency: 2.352572145545797e-4
allele num: 12752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+140T>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-66T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+140T>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.577T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+140T>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+140T>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3069T>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-55161320-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161320
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161320
    reference: chr 1
allele count: 1
allele frequency: 1.067691650651292e-4
allele num: 9366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+157C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.594C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3086C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-49C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+157C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+157C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+157C>G
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

1-55161321-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161321
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161321
    reference: chr 1
allele count: 1
allele frequency: 1.071352046282408e-4
allele num: 9334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.595C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+158C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-48C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+158C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+158C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+158C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3087C>G
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-55161330-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55161330
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55161330
    reference: chr 1
allele count: 1
allele frequency: 1.235177865612648e-4
allele num: 8096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2964+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000493533
  gene symbol: MROH7
  hgvsc: ENST00000493533.1:n.604C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+167C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1553+3096C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+167C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1097-39C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+167C>G
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+167C>G
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2964+167C>G
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

1-55163299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55163299
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55163299
    reference: chr 1
allele count: 1
allele frequency: 6.904170118751726e-5
allele num: 14484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+2136C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2965-27C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.435C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1257-27C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+2136C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2965-27C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+2136C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+2136C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-2695C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+2136C>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-55163334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55163334
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55163334
    reference: chr 1
allele count: 6
allele frequency: 3.913383772501957e-4
allele num: 15332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+2171C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-2660C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+2171C>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1265C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2973C>T
  hgvsp: ENST00000395690.2:c.2973C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2973C>T
  hgvsp: ENST00000339553.5:c.2973C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.470C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+2171C>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+2171C>T
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys991Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

1-55163335-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55163335
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55163335
    reference: chr 1
allele count: 2
allele frequency: 1.303441084462982e-4
allele num: 15344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.2974G>A
  hgvsp: ENSP00000379044.2:p.Glu992Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*544+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.471G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.2974G>A
  hgvsp: ENSP00000343211.5:p.Glu992Lys
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1236+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1518+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1096+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1266G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1668+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1096+2172G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1096+2172G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2964+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-2659G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*750+2172G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2964+2172G>A
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu992Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

1-55163359-CTTAGGTGAGTTAAGGGGAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55163359
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55163340
    reference: chr 1
allele count: 1
allele frequency: 6.502796202367018e-5
allele num: 15378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: splice donor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3001_3002+17delAGGTGAGTTAAGGGGAATT
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: CTTAGGTGAGTTAAGGGGAA
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-55165696-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55165696
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55165696
    reference: chr 1
allele count: 1
allele frequency: 2.420135527589545e-4
allele num: 4132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1237-307G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2965-298G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1295-53G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.2832G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2965-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1097-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*751-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*545-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000271723
  ensembl transcript: ENST00000460155
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000460155.1:n.728G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.3003-46G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1519-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1669-298G>C
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1097-298G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1097-298G>C
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.3003-53G>C
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

1-55165699-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55165699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55165699
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 4112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000271723
  ensembl transcript: ENST00000460155
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000460155.1:n.731G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1519-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1097-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.3003-50G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1097-295G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2965-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.3003-43G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.2835G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1097-295G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1295-50G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2965-295G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*545-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1237-304G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1669-295G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*751-295G>T
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

1-55165711-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55165711
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55165711
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 4120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1097-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1237-292G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*751-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1669-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2965-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.2847G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1295-38G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000271723
  ensembl transcript: ENST00000460155
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000460155.1:n.743G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1097-283G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*545-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.3003-38G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2965-283G>T
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.3003-31G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1519-283G>T
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1097-283G>T
  variant of: http://identifiers.org/hgnc/49180
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

1-55165727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55165727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 55165727
    reference: chr 1
allele count: 1
allele frequency: 2.36854571293226e-4
allele num: 4222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000387048
  ensembl transcript: ENST00000409996
  gene symbol: MROH7
  hgvsc: ENST00000409996.1:c.1669-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000271723
  ensembl transcript: ENST00000460155
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000460155.1:n.759G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184313
  ensembl transcript: ENST00000371287
  gene symbol: MROH7
  hgvsc: ENST00000371287.3:n.2863G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000404780
  ensembl transcript: ENST00000438846
  gene symbol: MROH7
  hgvsc: ENST00000438846.1:c.*1295-22G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000394373
  ensembl transcript: ENST00000413188
  gene symbol: MROH7
  hgvsc: ENST00000413188.1:c.*751-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000388181
  ensembl transcript: ENST00000422659
  gene symbol: MROH7
  hgvsc: ENST00000422659.1:c.*1097-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000379044
  ensembl transcript: ENST00000395690
  gene symbol: MROH7
  hgvsc: ENST00000395690.2:c.3003-15G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000343211
  ensembl transcript: ENST00000339553
  gene symbol: MROH7
  hgvsc: ENST00000339553.5:c.3003-22G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000392238
  ensembl transcript: ENST00000425300
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000425300.2:c.*1097-267G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000442333
  ensembl transcript: ENST00000545244
  gene symbol: MROH7
  hgvsc: ENST00000545244.1:c.1554-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000402209
  ensembl transcript: ENST00000440047
  gene symbol: MROH7
  hgvsc: ENST00000440047.1:c.*545-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000410192
  ensembl transcript: ENST00000414150
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000414150.2:c.2965-267G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000401130
  ensembl transcript: ENST00000454855
  gene symbol: MROH7
  hgvsc: ENST00000454855.2:c.1519-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000396622
  ensembl transcript: ENST00000421030
  gene symbol: MROH7
  hgvsc: ENST00000421030.2:c.2965-267G>A
  variant of: http://identifiers.org/hgnc/24802
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271723
  ensembl protein: ENSP00000475315
  ensembl transcript: ENST00000606515
  gene symbol: MROH7-TTC4
  hgvsc: ENST00000606515.1:c.*1097-267G>A
  variant of: http://identifiers.org/hgnc/49180
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184313
  ensembl protein: ENSP00000399703
  ensembl transcript: ENST00000440217
  gene symbol: MROH7
  hgvsc: ENST00000440217.1:c.*1237-276G>A
  variant of: http://identifiers.org/hgnc/24802
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-55165734-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55165734
    reference: chr 1
allele count: 1
allele frequency: 2.319109461966605e-4
allele num: 4312
alternate allele: A
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
hgvs: c.3003-8T>A
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 21
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7913
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9266
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1010
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8737
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.713502398903358e-5
allele num: 58360
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.745e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.226344e6

VQSLOD
type: SiteQuality
SIO_000300: -1.063e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

GenotypeDepth
all individuals: 224
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 138
bin: 3.75e1
variant carriers: 23

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

GenotypeDepth
all individuals: 5
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1393
bin: 3.25e1
variant carriers: 19

GenotypeDepth
all individuals: 27
bin: 9.75e1
variant carriers: 10

GenotypeDepth
all individuals: 9409
bin: 2.75e1
variant carriers: 37

GenotypeDepth
all individuals: 14
bin: 4.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3000
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 693
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 2.75e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 2.596439169139466e-2
allele num: 8088
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Other
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 3.925417075564279e-4
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.805962022731914e-5
allele num: 58772
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 60280
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South Asian
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Other
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 (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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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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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.653986106516705e-5
allele num: 60460
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.58e-1

ClippingRankSum
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SIO_000300: 3.68e-1

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

Latino
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allele frequency: 0.0e0
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European (Finnish)
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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)
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allele count: 1
allele frequency: 1.636393388970709e-5
allele num: 61110
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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QD
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.1e-3

BaseQRankSum
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SIO_000300: -7.75e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61238
num of homozygotes: 0

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

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

Latino
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allele frequency: 3.755163349605708e-4
allele num: 10652
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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num of homozygotes: 0

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

FS
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SIO_000300: 0.0e0

DP
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InbreedingCoeff
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SIO_000300: -1.0e-3

MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.213e0

QD
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VQSLOD
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SIO_000300: 6.8e-1

MQRankSum
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SIO_000300: -6.8e-1

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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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

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

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

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

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

South Asian
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allele frequency: 1.373815084489628e-4
allele num: 14558
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -9.0e-4

VQSLOD
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SIO_000300: -2.098e-1

BaseQRankSum
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SIO_000300: -2.566e0

DP
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SIO_000300: 1.278752e6

MQRankSum
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SIO_000300: 1.05e0

ReadPosRankSum
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SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -1.36e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

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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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.633826749011535e-5
allele num: 61206
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10648
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

ClippingRankSum
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SIO_000300: -1.93e-1

MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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SIO_000300: -1.95e-1

QD
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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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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

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 61224
num of homozygotes: 0

East Asian
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Other
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Latino
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DP
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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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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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 61218
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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African
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East Asian
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Other
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VQSLOD
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BaseQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 11

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

East Asian
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Other
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African
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allele frequency: 5.658171615618424e-2
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European (Non-Finnish)
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allele frequency: 2.122656913330285e-4
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South Asian
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Latino
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 9.386146048432514e-5
allele num: 10654
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 1.632173402102239e-5
allele num: 61268
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Other
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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MQ
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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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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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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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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allele count: 0
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Latino
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Other
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South Asian
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QD
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele num: 59986
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South Asian
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Other
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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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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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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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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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DP
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58774
num of homozygotes: 0

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

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

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

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

East Asian
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allele count: 3
allele frequency: 3.919519205644108e-4
allele num: 7654
num of homozygotes: 0

MQRankSum
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SIO_000300: 3.07e-1

VQSLOD
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QD
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SIO_000300: 1.055e1

ReadPosRankSum
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ClippingRankSum
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FS
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SIO_000300: 1.244e0

BaseQRankSum
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SIO_000300: -1.283e0

InbreedingCoeff
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SIO_000300: 2.1e-3

MQ
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SIO_000300: 6.0e1

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5120
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10036
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: 1
allele frequency: 1.725625539257981e-5
allele num: 57950
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 frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.167e0

InbreedingCoeff
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SIO_000300: -1.6e-3

MQ
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DP
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SIO_000300: 1.189776e6

VQSLOD
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SIO_000300: -3.4e0

ClippingRankSum
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SIO_000300: 1.91e-1

ReadPosRankSum
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SIO_000300: -5.31e-1

MQRankSum
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SIO_000300: -1.052e0

QD
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SIO_000300: 1.98e0

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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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

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

East Asian
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.65123411713159e-4
allele num: 13694
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 8.84548703251601e-5
allele num: 56526
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.158432e6

InbreedingCoeff
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SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 3.143e0

MQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

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

Other
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South Asian
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

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

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

African
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Latino
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allele num: 9234
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East Asian
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European (Finnish)
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MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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SIO_000300: -1.1e-3

BaseQRankSum
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ClippingRankSum
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SIO_000300: 5.69e-1

ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 5.611672278338945e-5
allele num: 53460
num of homozygotes: 0

African
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Latino
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
allele num: 4572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.704e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 1.083407e6

FS
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QD
type: SiteQuality
SIO_000300: 2.21e1

ReadPosRankSum
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SIO_000300: 1.58e-1

InbreedingCoeff
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SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

ClippingRankSum
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SIO_000300: -7.9e-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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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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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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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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allele frequency: 2.917152858809801e-4
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European (Non-Finnish)
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allele frequency: 1.872028155303456e-5
allele num: 53418
num of homozygotes: 0

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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MQRankSum
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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DP
type: SiteQuality
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 7.53e-1

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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East Asian
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allele num: 5688
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Other
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 2.225585328941511e-5
allele num: 44932
num of homozygotes: 0

European (Finnish)
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BaseQRankSum
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DP
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FS
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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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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East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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South 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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MQ
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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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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European (Finnish)
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South Asian
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East 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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QD
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FS
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele frequency: 2.279358132749818e-5
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MQ
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VQSLOD
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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allele frequency: 4.806767929244376e-5
allele num: 41608
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South Asian
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ReadPosRankSum
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QD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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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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Other
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European (Non-Finnish)
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allele frequency: 4.870920603994155e-5
allele num: 41060
num of homozygotes: 0

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

South Asian
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allele frequency: 2.183882943874208e-4
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East Asian
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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ReadPosRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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QD
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VQSLOD
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FS
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MQRankSum
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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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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African
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East Asian
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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 num: 10910
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Other
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Latino
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South Asian
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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South Asian
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African
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Latino
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Other
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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African
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South Asian
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ReadPosRankSum
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FS
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DP
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VQSLOD
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QD
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MQRankSum
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MQ
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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South Asian
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African
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ClippingRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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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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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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African
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South Asian
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ClippingRankSum
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VQSLOD
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FS
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MQ
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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African
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Other
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Latino
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South Asian
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European (Finnish)
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East Asian
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QD
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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QD
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Latino
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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MQRankSum
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MQ
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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GenotypeQuality
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African
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European (Finnish)
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MQ
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VQSLOD
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DP
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type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

DP
type: SiteQuality
SIO_000300: 1.07708e5

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.29e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

QD
type: SiteQuality
SIO_000300: 1.727e1

FS
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.641e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.111e0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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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: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2490
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.19e-2

DP
type: SiteQuality
SIO_000300: 1.07823e5

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

VQSLOD
type: SiteQuality
SIO_000300: -1.019e0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 4.25e1
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: 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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bin: 2.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.840000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 1.10039e5

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-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
all individuals: 15760
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GenotypeDepth
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GenotypeDepth
all individuals: 18
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GenotypeDepth
all individuals: 202
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variant carriers: 1

GenotypeDepth
all individuals: 131
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GenotypeDepth
all individuals: 3
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 265
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 55
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 42
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 222
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.291989664082687e-3
allele num: 774
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

FS
type: SiteQuality
SIO_000300: 2.398e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.969e-1

QD
type: SiteQuality
SIO_000300: 1.092e1

DP
type: SiteQuality
SIO_000300: 1.17997e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0